react

[ASAP] 4-Nitrophenol Reduction: Probing the Putative Mechanism of the Model Reaction

ACS Catalysis
DOI: 10.1021/acscatal.0c00725




react

[ASAP] A Thiadiazole-Based Covalent Organic Framework: A Metal-Free Electrocatalyst toward Oxygen Evolution Reaction

ACS Catalysis
DOI: 10.1021/acscatal.9b05470




react

[ASAP] A Complete Multisite Reaction Mechanism for Low-Temperature NH<sub>3</sub>-SCR over Cu-CHA

ACS Catalysis
DOI: 10.1021/acscatal.0c00440




react

[ASAP] Lattice Strain Induced by Linker Scission in Metal–Organic Framework Nanosheets for Oxygen Evolution Reaction

ACS Catalysis
DOI: 10.1021/acscatal.0c00989




react

[ASAP] Deciphering a Reaction Network for the Switchable Production of Tetrahydroquinoline or Quinoline with MOF-Supported Pd Tandem Catalysts

ACS Catalysis
DOI: 10.1021/acscatal.0c00899




react

[ASAP] Engineering Local and Global Structures of Single Co Atoms for a Superior Oxygen Reduction Reaction

ACS Catalysis
DOI: 10.1021/acscatal.0c00936




react

[ASAP] Catalytic Carbon–Carbon Bond Activation of Saturated and Unsaturated Carbonyl Compounds via Chelate-Assisted Coupling Reaction with Indoles

ACS Catalysis
DOI: 10.1021/acscatal.0c01245




react

[ASAP] Gold(I)-Catalyzed Highly Enantioselective [4 + 2]-Annulations of Cyclopentadienes with Nitrosoarenes via Nitroso-Povarov versus Oxidative Nitroso-Povarov Reactions

ACS Catalysis
DOI: 10.1021/acscatal.0c01293




react

[ASAP] Enhancing the Electrocatalytic Activity of Pd/M (M = Ni, Mn) Nanoparticles for the Oxygen Reduction Reaction in Alkaline Media through Electrochemical Dealloying

ACS Catalysis
DOI: 10.1021/acscatal.9b05499




react

[ASAP] Photoinduced Surface Activation of Semiconductor Photocatalysts under Reaction Conditions: A Commonly Overlooked Phenomenon in Photocatalysis

ACS Catalysis
DOI: 10.1021/acscatal.0c00462




react

[ASAP] Photoredox Catalysis: The Reaction Mechanism Can Adjust to Electronic Properties of a Catalyst

ACS Catalysis
DOI: 10.1021/acscatal.0c00200




react

[ASAP] ß-Cyclodextrin–NHC–Gold(I) Complex (ß-ICyD)AuCl: A Chiral Nanoreactor for Enantioselective and Substrate-Selective Alkoxycyclization Reactions

ACS Catalysis
DOI: 10.1021/acscatal.0c00127




react

A fluorescence-positioned hybridization chain reaction system for sensitive detection of Salmonella in milk

Anal. Methods, 2020, 12,1958-1965
DOI: 10.1039/D0AY00184H, Paper
Guotai Yang, Shuang Yu, Yang Liu, Jin Huang, Qianying Li, Zoraida P. Aguilar, Hengyi Xu
In this study, a fluorescence-positioned hybridization chain reaction (HCR) system for the detection of single-stranded DNA (ssDNA) specific to Salmonella was developed.
The content of this RSS Feed (c) The Royal Society of Chemistry




react

Chiral separations with crosslinked cellulose derivatives attached onto hybrid silica monolith particles via thiol-ene click reaction

Anal. Methods, 2020, Accepted Manuscript
DOI: 10.1039/D0AY00772B, Paper
Yuhong Zhou, Qian Liang, Zhilun Zhang, Zhaodi Wang, Mingxian Huang
Hybrid silica monolith containing vinyl groups was synthesized by a sol-gel method and then ground and treated, yielding silica particles with 3-5 μm in particles size and 10-20 nm in...
The content of this RSS Feed (c) The Royal Society of Chemistry




react

Rapid and colorimetric detection of nucleic acids based on entropy-driven circuit and DNAzyme mediated autocatalytic reaction

Anal. Methods, 2020, Accepted Manuscript
DOI: 10.1039/D0AY00341G, Paper
Hongli Shi, Jianyuan Dai, fang Wang, Yushun Xia, Dan Xiao, Cuisong Zhou
In this work, a novel, rapid and enzyme-free colorimetric biosensor for nucleic acids detection has been developed based on entropy-driven circuit (EDC) and DNAzyme mediated autocatalytic reaction. Upon sensing of...
The content of this RSS Feed (c) The Royal Society of Chemistry




react

[ASAP] 3-Nitrene-2-formylthiophene and 3-Nitrene-2-formylfuran: Matrix Isolation, Conformation, and Rearrangement Reactions

The Journal of Physical Chemistry A
DOI: 10.1021/acs.jpca.9b11638




react

[ASAP] Reaction Mechanism of the Isomerization of Monoterpene Epoxides with Fe<sup>3+</sup> as Active Catalytic Specie: A Computational Approach

The Journal of Physical Chemistry A
DOI: 10.1021/acs.jpca.9b09622




react

[ASAP] Reactivity Parameters and Substitution Effect in Organic Acids

The Journal of Physical Chemistry A
DOI: 10.1021/acs.jpca.9b10258




react

[ASAP] Organocatalysis by Halogen, Chalcogen, and Pnictogen Bond Donors in Halide Abstraction Reactions: An Alternative to Hydrogen Bond-Based Catalysis

The Journal of Physical Chemistry A
DOI: 10.1021/acs.jpca.0c01060




react

Experimental observation of boundary-driven oscillations in a reaction–diffusion–advection system

Soft Matter, 2020, 16,4243-4255
DOI: 10.1039/C9SM02291K, Paper
Open Access
  This article is licensed under a Creative Commons Attribution 3.0 Unported Licence.
Torsten Eckstein, Estefania Vidal-Henriquez, Azam Gholami
Boundary-driven oscillations are observed experimentally in a reaction-diffusion-advection system, namely in the signaling population of Dictyostelium discoideum cells.
The content of this RSS Feed (c) The Royal Society of Chemistry




react

Extreme reactions: radical right mobilization in Eastern Europe / Lenka Bustikova, Arizona State University

Dewey Library - JC573.2.E852 B88 2020




react

Indicted by SC panel, Justice Ganguly reacts: Not true, can't happen

Justice Ganguly is under pressure to resign as the chief of West Bengal Human Rights Commission.




react

Twitter reaction: Disappointment over SC's 'gay sex illegal' order

Supreme Court's verdict stating that Gay Sex is illegal has triggered a debate.




react

Heterogeneous electrochemical reactions taking place on metallic iron in ammoniacal-carbonate solutions containing dissolved nickel, cobalt, copper and thiosulfate ions / Anna d'Aloya de Pinilla

D'Aloya de Pinilla, Anna, author




react

The extractive metallurgy of brannerite : leaching kinetics, reaction mechanisms and mineralogical transformations / Rorie Alexander Gilligan

Gilligan, Rorie Alexander, author




react

061 JSJ Functional Reactive Programming with Juha Paananen and Joe Fiorini

Panel Juha Paananen (twitter github blog) Joe Fiorini (twitter github blog) AJ O’Neal (twitter github blog) Jamison Dance (twitter github blog) Joe Eames (twitter github blog) Merrick Christensen (twitter github) Charles Max Wood (twitter github Teach Me To Code Rails Ramp Up) Discussion 01:20 - Joe Fiorini Introduction Interaction Developer at Designing Interactive in Cleveland, OH 01:42 - Juha Paananen Introduction Software Developer at Reaktor in Helsinki, Finland 02:30 - Functional Reactive Programming (FRP) vs Functional Programming 057 JSJ Functional Programming with Zach Kessin 04:25 - Declarative Programming 05:55 - Map and Filter 07:05 - bacon.js Flapjax 09:10 - Mapping and filtering event streams 10:40 - Asynchronicity and Promises 14:28 - Using FRP ReactiveCocoa Complex UIs TodoMVC with Bacon.js, Backbone.js and Transparency.js by pyykiss 20:02 - Ember.js and FRP 22:04 - MVC frameworks and FRP Juha Paananen: FRP, Bacon.js and stuff: Chicken, Egg and Bacon.js 24:35 - Learning FRP 25:49 - Where did FRP come from? What is (functional) reactive programming? - Stack Overflow Conal Elliott: Composing Reactive Animations Haskell Reactive-banana - HaskellWiki 29:07 - Going beyond visual media substack/stream-handbook 32:18 - Wrappers 33:31 - How to build things with FRP libraries Juha Paananen @ MLOC.JS: Functional Reactive Programming in JavaScript using Bacon.js Picks SlideShare: Functional Reactive Programming in JavaScript (AJ) Valve: The AI Systems of Left 4 Dead by Michael Booth (Jamison) programming is terrible (Jamison) Simple Made Easy: Rich Hickey (Jamison) AngularJS Fundamentals (Joe's Pluralsight Course) (Joe) Open Source Bridge (Joe) That Conference (Joe) Star Trek: Into Darkness (Joe) ServerBear (AJ) rainwave (AJ) rwbackend (AJ) Mesa Boogie Lone Star Guitar Amplifier (Merrick) backburner.js (Merrick) messageformat.js (Merrick) Digital Ocean (Chuck) Emacs (Chuck) emacs_libs (Chuck) Tmux (Chuck) GitLab (Chuck) Flight by Twitter (Joe F.) Ember.js (Joe F.) CodeMash (Joe F.) fantasy-land (Juha) The Bacon.js postings featuring Phil Roberts (Juha) Iron Sky (Juha) Reaktor Dev Day (Juha) Next Week Dojo with Dylan Schiemann Transcript MERRICK:  How come nobody acknowledges when I talk? What about that? JAMISON:  That’s a deeper problem than a microphone. [Hosting and bandwidth provided by the Blue Box Group. Check them out at Bluebox.net.]  [This episode is sponsored by Component One, makers of Wijmo. If you need stunning UI elements or awesome graphs and charts, then go to Wijmo.com and check them out.]  CHUCK:  Hey everybody, and welcome to Episode 61 of the JavaScript Jabber Show. This week on our panel, we have AJ O’Neal. AJ:  Yo, yo, yo. Coming at you live from Iowa. CHUCK:  Again? AJ:  Oh, I guess I was there last time, huh? It’ll be New York soon. CHUCK:  We have Jamison Dance. JAMISON:  Howdy, guys. CHUCK:  Joe Eames. JOE E:  Hey there. CHUCK:  Merrick Christensen. MERRICK:  What’s up? CHUCK:  I’m Charles Max Wood from DevChat.tv. This week, we have two special guests. We have Joe Fiorini. JOE F:  Hello everyone. CHUCK:  And Juha Paananen. JUHA:  Yeah. Hi everybody. Juha Paananen. CHUCK:  Thank you for straightening that up for me. We’re going to have you guys introduce yourself real quick, since you haven’t been on the show before. Joe, why don’t you start us off? JOE F:  Sure. My name is Joe Fiorini and I am an Interaction Developer at Designing Interactive in Cleveland, Ohio. I do a decent amount of JavaScript development every week. I’ve discovered Functional Reactive Programming three or four months ago and it’s changed my world. CHUCK:  Awesome. And Juha, do you want to introduce yourself as well? JUHA:  Yeah, why not? I’m Juha. I’m from Finland. Helsinki.




react

073 JSJ React with Pete Hunt and Jordan Walke

Panel Pete Hunt (twitter github blog) Jordan Walke (twitter github) Joe Eames (twitter github blog) AJ O’Neal (twitter github blog) Jamison Dance (twitter github blog) Merrick Christensen (twitter github) Charles Max Wood (twitter github Teach Me To Code Rails Ramp Up) Discussion 01:34 - Pete Hunt Introduction Instagram Facebook 02:45 - Jordan Walke Introduction 04:15 - React React - GitHub 06:38 - 60 Frames Per Second 09:34 - Data Binding 12:31 - Performance 17:39 - Diffing Algorithm 19:36 - DOM Manipulation 23:06 - Supporting node.js 24:03 - rendr 26:02 - JSX 30:31 - requestAnimationFrame 34:15 - React and Applications 38:12 - React Users Khan Academy 39:53 - Making it work Picks Ben Mabey: Clojure Plain & Simple (Jamison) JSConf 2013 Videos (Jamison) Kittens (Jamison) PBS Idea Channel (AJ) Free Trial SSL (AJ) OSX Wifi Volume Remote Control (AJ) js-git (Merrick) vim-airline (Merrick) MLS LIVE (Joe) Seraphina by Rachel Hartman (Joe) ng-conf (Joe) Hire Chuck (Chuck) GoToMeeting (Chuck) ScreenFlow (Chuck) syriandeveloper (Pete) jsFiddle (Pete) Hotel Tonight (Pete) Green Flash Brewery Beer: Palate Wrecker (Jordan) All Things Vim (Jordan) Next Week Grunt.js with Ben Alman Transcript JAMISON:  Joe is Merrick’s personal assistant. CHUCK:  [Laughter] MERRICK:  No, we’re just in this little room and he had, he was like, “Yeah” JOE:  Want me to freshen up your coffee, sir? [Chuckles] JAMISON:  Feed me some tacos, Joe. [Laughter] [Hosting and bandwidth provided by the Blue Box Group. Check them out at BlueBox.net.]  [This episode is sponsored by Component One, makers of Wijmo. If you need stunning UI elements or awesome graphs and charts, then go to Wijmo.com and check them out.]  [This podcast is sponsored by JetBrains, makers of WebStorm. Whether you’re working with Node.js or building the front end of your web application, WebStorm is the tool for you. It has great code quality and code exploration tools and works with HTML5, Node, TypeScript, CoffeeScript, Harmony, LESS, Sass, Jade, JSLint, JSHint, and the Google Closure Compiler. Check it out atJjetBrains.com/WebStorm.] CHUCK:  Hey everybody and welcome to episode 73 of the JavaScript Jabber Show. This week on our panel, we have Joe Eames. JOE:  Hey there. CHUCK:  AJ O’Neal. AJ:  Live again from Provo. CHUCK:  Jamison Dance. JAMISON:  Hey friends. CHUCK:  Merrick Christensen. MERRICK:  Hey guys. CHUCK:  I’m Charles Max Wood from DevChat.TV and we have two special guests this week. Pete Hunt. PETE:  Hey guys. CHUCK:  And Jordan Walke. JORDAN:  Hi. CHUCK:  Since you guys haven’t been on the show before, do you want to introduce yourselves? We’ll have Pete go first. PETE:  Sure. So my name’s Pete. I work on general React stuff these days. But my day job is building the Instagram web experience. If you go to Instagram.com, we have a bunch of frontend stuff you can play with and a bunch of backend infrastructure that supports all that. That’s what I mostly work on. We’re big users of React at Instagram so I ended up contributing a lot to the React core as well. JAMISON:  So did you come from Instagram or from Facebook and then to work on Instagram? PETE:  Well it was actually a pretty good story just in terms of the integration of the two companies. I was originally at Facebook for a couple of years and we acquired Instagram and they came in and they wanted to build a web presence. Facebook’s core competency is definitely web technologies and Instagram hasn’t historically focused on that. So we were able to take the Facebook web expertise and get Instagram up and running really quickly. I came from the Facebook side but the team is still very much a separate team, their own building, that kind of thing. So that’s my background. CHUCK:  Awesome. JAMISON:  Sweet. CHUCK:  And Jordan?




react

146 JSJ React with Christopher Chedeau and Jordan Walke

The panelists talk to Christopher Chedeau and Jordan Walke about React.js Conf and React Native.




react

157 Moving Your Rendering Engine to React with Amit Kaufman and Avi Marcus

02:43 - Amit Kaufman Introduction

03:07 - Avi Marcus Introduction

04:35 - Why Move Your Rendering Engine to React?

07:25 - Using JavaScript

09:57 - Business Process and Progression (Getting Managerial Approval)

12:46 - Manipulation

15:11 - Layout and Performance

  • Measuring and Patching

20:21 - Building Client-Side Applications in General

  • Abstraction
  • Make Code Predictable and Clear
  • Have a Goal

26:00 - Events

29:30 - Storage

  • Lazy Components

31:31 - Immutability

34:36 - Flux and Keeping Code Maintainable

  • Packages

38:19 - Two-way Data Binding

Picks

Notes on the book "Art & Fear" by David Bayles & Ted Orland (Jamison)
Papers (Jamison)
Dynamo: Amazon’s Highly Available Key-value Store (Jamison)
LDS Conference Talks (AJ)
Stephen Young: Why your code is so hard to understand (Aimee)
Kombucha (Aimee)
Pascal Precht: Integrating Web Components with AngularJS (Pascal)
Template Syntax Constraints and Reasoning (Design Doc) (Pascal)
RUNNING WITH RIFLES (Joe)
[Pluralsight Webinar] AngularJS 2.0: What you need to know with Joe (Joe)
Whiplash (Amit)
Dan Ariely: What makes us feel good about our work? (Amit)
React Templates (Amit)
Esprima (Avi)
Big Hero 6 (Avi)

 

Check out and sign up to get new on React Rally: A community React conference on August 24th and 25th in Salt Lake City, Utah!




react

179 JSJ redux and React with Dan Abramov

02:25 - Dan Abramov Introduction

02:43 - Dan’s Background and Journey Into Building Stuff with React

05:48 - redux and React    

10:07- The Elm Programming Language

12:19 - Reducers

14:04 - Hot Reloading

17:50 - “React makes you a better JavaScript developer.”

22:10 - Time Travel

28:26 - Storing Data and Managing State

34:43 - [Patreon] Support Dan Abramov Creating Redux and React Hot Loader

36:24 - react-transform

41:34 - Using redux outside React

43:52 - Editors and Programmer Productivity

45:35 - Future Plans

Picks

The OAuth2 RFC (Aimee)
Michael Ries: Hiring Apprentices (Jamison)
@sebmck: "Sometimes having email history isn't always a good thing..." (Jamison)
Metal Gear Solid 5: The Phantom Pain (Jamison)
Firefly (Joe)
The Elm Programming Language (Joe)
Google Keep (Dave)
15 Minute Podcast Listener chat with Charles Wood (Chuck)
Pebble Time (Chuck)
100 Days of Burpees (Chuck)
Broad City (Dan)
Jamie xx: In Colour (Dan)
Cycle.js (Dan)




react

227 JSJ Fostering Community Through React with Benjamin Dunphy, Berkeley Martinez, and Ian Sinnott

03:08 - Benjamin Dunphy Introduction

04:07 - Berkeley Martinez Introduction

04:19 - Ian Sinnott Introduction

05:19 - The React Codebase

12:38 - Other Important Parts of the React Ecosystem

14:22 - The Angular vs the React Ecosystem and Community

22:07 - Community

Developer Experience

26:56 - Getting Connected to the React Community

29:34 - Conferences

33:28 - Technology From the Community

40:19 - The Future of React

42:39 - Starting More Communities

 

Picks




react

228 JSJ React Native with Nader Dabit and Mike Grabowski

Code-sharing between mobile and web apps with React Native

Using native code and Javascript

What to know about developing with React Native

The importance of tooling

Live and hot-reloading

Updating your app on the fly

Possible difficulties faced by transitioning to React Native

Bridging between native API’s and React Native

Writing apps in Swift or React Native

The future of React Native

How to start a React Native project

 

Resources:

Frontend Masters

Hired.com

Rollbar

Microsoft Code Push

React Native Radio Episode 8

Tadeu Zagallo’s Website




react

237 JSJ CLls - Ember Angular and React with Tracy Lee

TOPICS:

3:57 The exciting facets of CLI’s

8:25 Advantages of CLI projects

11:25 Coding in RAILS

14:18 Disagreeing with conventions encoded in a CLI

19:30 How REACT CLI functions

20:43 Is Ember cheating by using REACT CLI?

26:52 Which CLI is easiest to use

29:00 How to add commands to a CLI

34:00 The future of current CLI’s

35:30 How well CLI’s are working for their respective communities

37:00 The impact of WebPac

PICKS:

“How Break Points are Set” Hacker News Article

Chocolate Mint Tea

Ten Things Wise Parents Know Book

Strong Fathers, Strong Daughters Book

Boys Should Be Boys Book

“How Half of America Lost its Effing Mind” Blog Post

Elementary TV Show

Recommendation Form for Topics and Guests

Amazon Smile

Angular Cruise

Sweet Licorice Mint Tea by Choice Organic Teas

Van’s Nintendo Sneakers

RESOURCES AND CONTACT INFO:

Tracy's E-mail




react

JSJ 245 Styled Components and react-boilerplate with Max Stoiber

On today's episode, Aimee and Chuck welcome Maximillian "Max" Stoiber to the show. Max hails from Austria and is an expert in open source development at Think Mill. Tune in to JSJ 245 Styled Components and React-Boilerplate with Max Stoiber.




react

JSJ 248 Reactive Programming and RxJS with Ben Lesh

On today's episode, Charles Max Wood, Joe Eames, and Tracy Lee discuss Reactive Programming and RxJS with Ben Lesh. Ben works at Netflix and also has a side job for Rx Workshop with Tracy. He is the lead author of RxJS 5. Tune in to learn more about RxJS!




react

JSJ 269 Reusable React and JavaScript Components with Cory House

JSJ 269 Reusable React and JavaScript Components with Cory House

On today’s episode of JavaScript Jabber, we have panelists Joe Eames, Aimee Knight, Charles Max Wood, and playing the part of both host and guest, Cory House. Encourage your team to investigate reusable components, whether that’d be React, Angular, Vue, or Ember. Tune in!

[00:01:35] – Overview

We can finally write reusable components that it is really lightweight. It doesn’t take much framework-specific code to get things done.

Around 3 years ago, the idea of web component standard was all front-end developers could share our components with each other whether someone is in Angular or React. Web components continue to be an interesting standard but people continue to reach for JavaScript libraries instead – React, Angular, Vue. 

[00:04:50] – Browser support issue

The story in JavaScript libraries is easier. You have more power, more flexibility, more choices, and get superior performance, in certain cases, by choosing a JavaScript library over the standard right now. If you try to use the web components standard, you have to Polyfill-in some features so you can run things across browser. You also won’t get JavaScript features like intelligently splitting bundles and lazy load different components.

Whether you’re in Angular or React, you have this model of putting your data in your curly braces. That setup is non-existent in standardized web components. You have to play the game of putting and pulling data into and out the DOM using DOM selectors. You actually take a step backward in developer ergonomics when you choose to leverage the platform instead.

[00:07:50] – Polymer

The reason that Polymer is useful is it adds some goodness on top of web components. One of those things is that it makes it easier to bind in data and not having to do things like writing a DOM query to be able to get your hands on this div and put this text inside of it. With Polymer, you can do something that feels more like Angular, where you can put in your curly braces and just bind in some data into that place. Polymer ends up adding some nice syntactic sugar on top of the web components standard just to make it easier to create web components. Polymer is also used to bundle in Polyfill for the features across browser.   

[00:14:20] – Standards are dead

No. The standard itself has been embraced at different levels by different libraries. What you can see for the near future is popular libraries leveraging pieces of the web components platform to do things in a standard-spaced way. Effectively, Angular, Vue, Aurelia, are going to be abstractions over the web components standard. Arguably the most popular way to do components today is React. But React completely ignores the web components standard. When you look at React, you can’t see what piece of the web components standard would fundamentally make React a better component library.

Cory can’t seem to run to anybody that is actually using the standard in production to build real applications. People continue to reach for the popular JavaScript libraries that we so often hear about.

[00:17:05] – Libraries making reusable components

There is a risk that it would have been a waste for people writing components on Angular, for React, for Vue. But it’s not necessarily safer writing on the web component standard when you have so few people leveraging that standard. There’s always the risk that that standard may shift as well.

As an example, Cory’s team created approximately 100 reusable components in React. If they end up moving to a hot new library, the components are really just functions that take parameters and contain HTML. There is little there

[00:21:20] – Why opt for reusable components

Reusable components are inherently useful in a situation where you’re going to be doing something more than once. If you think about any work that you do as a software developer, we’d like to think that we’re coming in and creating new things but often it is groundhogs day. There are all sorts of opportunities for reuse.

As a company, we want to encapsulate our forms in reusable components so it’s literally impossible for our software developers to do something that goes against our standard. That’s the power of reusable components.  

[00:31:20] – Rigid component vs. flexible component

As component developers, if we try to create a reusable component in a vacuum, bad things happen. If you’re going to do a reusable component, start by solving a specific problem on a given application. If we think that a component’s going to be useful in multiple places, we put it in a folder called reusable right there in our application source folder.

We try to follow that rule of three as well. If we’ve taken that component and used it in 3 places, that’s a good sign that we should extract it out, put it in our NPM package, that way, everybody has this centralized component to utilize. At that point, it has been tested. It’s been through the fire. People have used it in the real world in a few places so we can be confident that the API is truly flexible enough.

Be as rigid as you can upfront. Once you add features, it’s really hard to take features away. But it’s quite easy to add features later. If you start with something rigid, it’s easier to understand. It’s easier to maintain and you can always add a few more switches later.

[00:36:00] – Reusable components

The reason that we can’t reuse code is every time a new project comes up, people are spending up their own ideas rather than leveraging standards that should have been put in place previously.

We’ve had the technical ability to do this for a long time. We just haven’t been around long enough for consolidation to happen, for standardization to happen. You look at how quickly things are changing in our industry. For instance, a couple of years ago, everybody had pretty much decided that two-way binding was the way to build web applications. And then, React came along and shook that up. So today, you have different ways of thinking about that issue.

[00:42:45] – Component development on teams

Aimee’s team has component development and they’re using Angular 1.6. All of our base components are sitting in a seed application. We just go in when we want to create a new property and we just extend all of those components with specific functionalities that we need.

[00:47:45] – Mobile to web crossover

Cory’s team is creating React components but it’s not leveraged on a mobile application. But people use React Native components on the web. And in fact, if you use create-react-app today, you can do that right now. It’s wired up to work in React Native components. In that way, you can literally have these same components running on your Native mobile apps as you do on your web application.

[00:50:00] – Challenge

Cory’s challenge for everybody listening is sit down with your team and have a quick conversation about whether you think components make sense. Look back at the last few months of development and say, "if we have a reusable component library, what would be in it? How often have we found ourselves copying and pasting code between different projects? How much benefit would we get out of this story?"

Once you’ve realized the benefits of the component model, both in the way that makes you think about your application, in a way that it helps you move faster and faster over time, I really think you won’t go back to the old model. I’d encourage people to investigate reusable components, whether that’d be React, Angular, Vue or Ember.

Picks

Cory House

Joe Eames

Aimee Knight

Charles Max Wood

JSJ 269 Reusable React and JavaScript Components with Cory House

On today’s episode of JavaScript Jabber, we have panelists Joe Eames, Aimee Knight, Charles Max Wood, and playing the part of both host and guest, Cory House. Encourage your team to investigate reusable components, whether that’d be React, Angular, Vue, or Ember. Tune in!

[00:01:35] – Overview

We can finally write reusable components that it is really lightweight. It doesn’t take much framework-specific code to get things done.

Around 3 years ago, the idea of web component standard was all front-end developers could share our components with each other whether someone is in Angular or React. Web components continue to be an interesting standard but people continue to reach for JavaScript libraries instead – React, Angular, Vue. 

[00:04:50] – Browser support issue

The story in JavaScript libraries is easier. You have more power, more flexibility, more choices, and get superior performance, in certain cases, by choosing a JavaScript library over the standard right now. If you try to use the web components standard, you have to Polyfill-in some features so you can run things across browser. You also won’t get JavaScript features like intelligently splitting bundles and lazy load different components.

Whether you’re in Angular or React, you have this model of putting your data in your curly braces. That setup is non-existent in standardized web components. You have to play the game of putting and pulling data into and out the DOM using DOM selectors. You actually take a step backward in developer ergonomics when you choose to leverage the platform instead.

[00:07:50] – Polymer

The reason that Polymer is useful is it adds some goodness on top of web components. One of those things is that it makes it easier to bind in data and not having to do things like writing a DOM query to be able to get your hands on this div and put this text inside of it. With Polymer, you can do something that feels more like Angular, where you can put in your curly braces and just bind in some data into that place. Polymer ends up adding some nice syntactic sugar on top of the web components standard just to make it easier to create web components. Polymer is also used to bundle in Polyfill for the features across browser.   

[00:14:20] – Standards are dead

No. The standard itself has been embraced at different levels by different libraries. What you can see for the near future is popular libraries leveraging pieces of the web components platform to do things in a standard-spaced way. Effectively, Angular, Vue, Aurelia, are going to be abstractions over the web components standard. Arguably the most popular way to do components today is React. But React completely ignores the web components standard. When you look at React, you can’t see what piece of the web components standard would fundamentally make React a better component library.

Cory can’t seem to run to anybody that is actually using the standard in production to build real applications. People continue to reach for the popular JavaScript libraries that we so often hear about.

[00:17:05] – Libraries making reusable components

There is a risk that it would have been a waste for people writing components on Angular, for React, for Vue. But it’s not necessarily safer writing on the web component standard when you have so few people leveraging that standard. There’s always the risk that that standard may shift as well.

As an example, Cory’s team created approximately 100 reusable components in React. If they end up moving to a hot new library, the components are really just functions that take parameters and contain HTML. There is little there

[00:21:20] – Why opt for reusable components

Reusable components are inherently useful in a situation where you’re going to be doing something more than once. If you think about any work that you do as a software developer, we’d like to think that we’re coming in and creating new things but often it is groundhogs day. There are all sorts of opportunities for reuse.

As a company, we want to encapsulate our forms in reusable components so it’s literally impossible for our software developers to do something that goes against our standard. That’s the power of reusable components.  

[00:31:20] – Rigid component vs. flexible component

As component developers, if we try to create a reusable component in a vacuum, bad things happen. If you’re going to do a reusable component, start by solving a specific problem on a given application. If we think that a component’s going to be useful in multiple places, we put it in a folder called reusable right there in our application source folder.

We try to follow that rule of three as well. If we’ve taken that component and used it in 3 places, that’s a good sign that we should extract it out, put it in our NPM package, that way, everybody has this centralized component to utilize. At that point, it has been tested. It’s been through the fire. People have used it in the real world in a few places so we can be confident that the API is truly flexible enough.

Be as rigid as you can upfront. Once you add features, it’s really hard to take features away. But it’s quite easy to add features later. If you start with something rigid, it’s easier to understand. It’s easier to maintain and you can always add a few more switches later.

[00:36:00] – Reusable components

The reason that we can’t reuse code is every time a new project comes up, people are spending up their own ideas rather than leveraging standards that should have been put in place previously.

We’ve had the technical ability to do this for a long time. We just haven’t been around long enough for consolidation to happen, for standardization to happen. You look at how quickly things are changing in our industry. For instance, a couple of years ago, everybody had pretty much decided that two-way binding was the way to build web applications. And then, React came along and shook that up. So today, you have different ways of thinking about that issue.

[00:42:45] – Component development on teams

Aimee’s team has component development and they’re using Angular 1.6. All of our base components are sitting in a seed application. We just go in when we want to create a new property and we just extend all of those components with specific functionalities that we need.

[00:47:45] – Mobile to web crossover

Cory’s team is creating React components but it’s not leveraged on a mobile application. But people use React Native components on the web. And in fact, if you use create-react-app today, you can do that right now. It’s wired up to work in React Native components. In that way, you can literally have these same components running on your Native mobile apps as you do on your web application.

[00:50:00] – Challenge

Cory’s challenge for everybody listening is sit down with your team and have a quick conversation about whether you think components make sense. Look back at the last few months of development and say, "if we have a reusable component library, what would be in it? How often have we found ourselves copying and pasting code between different projects? How much benefit would we get out of this story?"

Once you’ve realized the benefits of the component model, both in the way that makes you think about your application, in a way that it helps you move faster and faster over time, I really think you won’t go back to the old model. I’d encourage people to investigate reusable components, whether that’d be React, Angular, Vue or Ember.

Picks

Cory House

Joe Eames

Aimee Knight

Charles Max Wood




react

JSJ 296: Changes in React and the license with Azat Mardan

Panel: 

Charles Max Wood

Cory House

Joe Eames

Aimee Knight

Special Guests: Azat Mardan

In this episode, JavaScript Jabber panelist speak with Azat Mardan. Azat is a return guest, previously on JSJ Episode 230. Azat is an author of 14 books on Node JS, JavaScript, and React JS. Azat works at Capital One on the technology team. Azat is the founder and creator of Node University.

Azat is on the show to talk about changes in React and licensing. Some of the topics cover Facebook,  licensing with React, using the wrong version of React, patent wars, and much more in-depth information on current events in React.

In particular, we dive pretty deep on:

  • Facebook - Licensing with React
  • Using the Wrong version of React in some companies
  • BSD licensing
  • Patent wars
  • Facebook developing React
  • Difference in Preact and Inferno
  • Rewriting applications
  • What did Capital One do about the changes?
  • React 16
  • Pure React
  • Was the BSD patents - Med and Sm Companies
  • Patents explained
  • React Developers at Facebook
  • Fiber - New Core Architecture
  • And much more!

Links:

Picks:

Cory

Charles

Aimee

Joe

Azat




react

JSJ 304: React: The Big Picture

Panel:

  • Charles Max Wood
  • Aimee Knight
  • Joe Eames
  • Cory House
  • AJ O'Neal

Special Guests: None

In this episode, the JavaScript Jabber panelists talk about React: The Big Picture, Cory’s course on Pluralsight and what React is all about. They discuss both the pros and cons when it comes to using React and when it would be the best to use this library. They also encourage programmers to use React in a more consistent way so that people can share components.

In particular, we dive pretty deep on:

  • What is React: The Big Picture course?
  • React
  • The frameworks work with each other
  • Reason and Elm
  • How to decide when using React is the best option?
  • React tradeoffs
  • JavaScript
  • React expects you to do a little more typing and work
  • React is very close to JavaScript
  • React pushes you towards a single file per component
  • React Round Up
  • Are the Code Mods as wonderful as they sound?
  • Angular
  • Create React App
  • What are Code Mods?
  • Lack of opinionated approach in React
  • Using React in a more consistent way
  • MobX and Redux
  • Start off using just plain React
  • When wouldn’t you want to use React?
  • And much, much more!

Links:

Picks:

Charles

Aimee

Joe

AJ




react

JSJ 407: Reactive JavaScript and Storybook with Dean Radcliffe

Dean is a developer from Chicago and was previously on React Round Up 083. Today he has come over to JavaScript Jabber to talk about reactive programming and Storybook. Reactive programming is the opposite of imperative programming, where it will change exactly when needed instead of change only when told to. Reactivity existed long before React, and Dean talks about his history with reactive programming. He illustrates this difference by talking about Trello and Jira. In Trello, as you move cards from swimlane to another swimlane, everyone on the board sees those changes right away. In Jira,  if you have 11 tabs open, and you update data in one tab, probably 10 of your tabs are stale now and you might have to refresh. Reactive programming is the difference between Trello and Jira.

The panel discusses why reactive JavaScript is not more widely used. People now tend to look for more focused tools to solve a particular part of the problem than an all in one tool like Meteor.js. Dean talks about the problems that Storybook solves. Storybook has hot reloading environments in frontend components, so you don’t need the backend to run. Storybook also allows you to create a catalogue of UI states. JC and Dean talk about how Storybook could create opportunities for collaboration between engineers and designers. They discuss some causes of breakage that automation could help solve, such as styles not being applied properly and internationalization issues. Dean shares how to solve some network issues, such as having operators in RxJs. RxJs is useful for overlapping calls because it was built with cancelability from the beginning. 

Dean talks about his tool Storybook Animate, which allows you to see what the user sees. Storybook is an actively updated product, and Dean talks about how to get started with it. The show concludes with Dean talking about some things coming down the pipe and how he is actively involved in looking for good general solutions to help people write bulletproof code. 

Panelists

  • JC Hiatt

With special guest: Dean Radcliffe

Sponsors

________________________________________________________________________________________________________________________

"The MaxCoders Guide to Finding Your Dream Developer Job" by Charles Max Wood will be out on November 20th on Amazon.  Get your copy on that date only for $1.

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Links

Follow DevChatTV on Facebook and Twitter

Picks

JC Hiatt:

Dean Radcliffe: 




react

Expeditious access of chromone analogues via a Michael addition-driven multicomponent reaction

Org. Chem. Front., 2020, 7,987-992
DOI: 10.1039/D0QO00145G, Research Article
Jie Lei, Yong Li, Liu-Jun He, Ya-Fei Luo, Dian-Yong Tang, Wei Yan, Hui-Kuan Lin, Hong-yu Li, Zhong-Zhu Chen, Zhi-Gang Xu
A Michael addition-driven four-component reaction (4-CR) with four Ugi inputs was developed and utilized for the synthesis of chromone derivatives and tetrazole substituted chromones under mild reaction conditions.
The content of this RSS Feed (c) The Royal Society of Chemistry




react

Oxidative N-heterocyclic carbene-catalyzed [3 + 3] annulation reaction of enals with benzofuran-3-ones: efficient access to benzofuran-fused δ-lactones

Org. Chem. Front., 2020, 7,1011-1015
DOI: 10.1039/D0QO00161A, Research Article
Zhan-Yong Wang, Ting Yang, Kai-Kai Wang, Rongxiang Chen, Menghan Liu, Hongxin Liu
A facile route to benzofuran-fused δ-lactones was developed via an N-heterocyclic carbene-catalyzed [3 + 3] annulation reaction, giving the expected products in high yields (up to 99%) with excellent enantioselectivities (up to 98% ee).
The content of this RSS Feed (c) The Royal Society of Chemistry




react

The key role of protodeauration in the gold-catalyzed reaction of 1,3-diynes with pyrrole and indole to form complex heterocycles

Org. Chem. Front., 2020, 7,997-1005
DOI: 10.1039/C9QO01544B, Research Article
Ioannis Stylianakis, Olalla Nieto Faza, Carlos Silva López, Antonios Kolocouris
The mechanism of indole and carbazole formation via a formal [4 + 2] cycloaddition strategy is dominated by the protodeauration step.
The content of this RSS Feed (c) The Royal Society of Chemistry




react

Pd/light-induced alkyl–alkenyl coupling reaction between unactivated alkyl iodides and alkenylboronic acids

Org. Chem. Front., 2020, Advance Article
DOI: 10.1039/D0QO00318B, Research Article
Hsin-Ju Huang, Yi-Ting Wang, Yen-Ku Wu, Ilhyong Ryu
Alkyl–alkenyl coupling reaction between unactivated alkyl iodides and 2-arylalkenylboronic acids utilizing a Pd/light combined system was studied.
To cite this article before page numbers are assigned, use the DOI form of citation above.
The content of this RSS Feed (c) The Royal Society of Chemistry




react

Direct organocatalytic asymmetric Michael reaction of fluorine hemiaminal-type nucleophile to 4-nitro-5-styrylisoxazoles

Org. Chem. Front., 2020, Advance Article
DOI: 10.1039/D0QO00348D, Research Article
Luyao Li, Bo Zhu, Huihui Fan, Zhiyong Jiang, Junbiao Chang
Herein, we report a chiral bifunctional thiourea catalyzed asymmetric Michael addition reaction between 2-(trifluoromethyl)oxazol-5(2H)-one as a direct C-2-position nucleophile to 4-nitro-5-styrylisoxazoles for the first time.
To cite this article before page numbers are assigned, use the DOI form of citation above.
The content of this RSS Feed (c) The Royal Society of Chemistry




react

Insights into N-heterocyclic carbene and Lewis acid cooperatively catalyzed oxidative [3 + 3] annulation reactions of α,β-unsaturated aldehyde with 1,3-dicarbonyl compounds

Org. Chem. Front., 2020, 7,1113-1121
DOI: 10.1039/D0QO00091D, Research Article
Xinghua Wang, Yang Wang, Jinshuai Song, Donghui Wei
N-Heterocyclic carbene and Lewis acid cooperatively catalyzed oxidative [3 + 3] annulation reactions of 1,3-dicarbonyl compounds have been systematically studied in theory.
The content of this RSS Feed (c) The Royal Society of Chemistry




react

Chiral strong Brønsted acid-catalyzed enantioselective addition reaction of simple olefins with ethyl glyoxylate

Org. Chem. Front., 2020, Advance Article
DOI: 10.1039/D0QO00448K, Research Article
Jun Kikuchi, Yuki Aizawa, Masahiro Terada
An enantioselective intermolecular addition reaction of 1,1,2-trisubstituted and 1,2- disubstituted simple olefins with ethyl glyoxylate was developed using F10BINOL-derived N-sulfonyl phosphoramide as a chiral strong Brønsted acid catalyst.
To cite this article before page numbers are assigned, use the DOI form of citation above.
The content of this RSS Feed (c) The Royal Society of Chemistry




react

A Vinylogous Michael Reaction of 2-Furanones Dimers to α, β-Unsaturated Nitroolefins for Constructing Chiral γ, γ-Disubstituted Butenolides

Org. Chem. Front., 2020, Accepted Manuscript
DOI: 10.1039/D0QO00376J, Research Article
Zhushuang Bai, Cairong Zhang, Yongyi Chen, Aiqin Liu, Xinyu Wang, Chuna Yan, Xuechao Liu, Xiaoru Zhang, Ying Li, Ye Yuan, Zemei Ge, Jingxiang Pang, Yongshuai Chai, Xin Wang, Runtao Li
An efficient bifunctional thiourea catalyzed asymmetric vinylogous Michael addition of 2-furanones dimers to α, β-unsaturated nitroolefins has been developed to give the functional chiral γ,γ-disubstituted butenolides in good yields (up...
The content of this RSS Feed (c) The Royal Society of Chemistry




react

Rhodium(III)-catalyzed synthesis of 3-trifluoromethylindanones from N-Methoxybenzamides via C-H activation and Claisen/Retro-Claisen reaction

Org. Chem. Front., 2020, Accepted Manuscript
DOI: 10.1039/D0QO00330A, Research Article
Satyasheel Sharma, Bharatkumar Chaudhary, Neeraj Kulkarni
The Rhodium(III)-catalyzed reaction of N-methoxybenzamides as a directing group with β-trifluoromethyl-α,β-unsaturated ketones is reported. The reaction involved sp2 C−H activation, followed by Claisen condensation involving C-N bond cleavage to form...
The content of this RSS Feed (c) The Royal Society of Chemistry




react

[ASAP] Contrasting Efficiency of Electron-Induced Reaction at Cu(110) in Aliphatic and Aromatic Bromides

Journal of the American Chemical Society
DOI: 10.1021/jacs.0c02851




react

[ASAP] Speciation of Cu Surfaces During the Electrochemical CO Reduction Reaction

Journal of the American Chemical Society
DOI: 10.1021/jacs.0c02354