vinyl

[ASAP] Copper-Catalyzed Oxyvinylation of Diazo Compounds

Organic Letters
DOI: 10.1021/acs.orglett.0c01150




vinyl

[ASAP] Selective Synthesis of Secondary Alkylboronates: Markovnikov-Selective Hydroboration of Vinylarenes with Bis(pinacolato)diboron Catalyzed by a Nickel Pincer Complex

Organic Letters
DOI: 10.1021/acs.orglett.0c01416




vinyl

[ASAP] Palladium-Catalyzed Regio- and Stereoselective Cross-Coupling of Vinylethylene Carbonates with Ketimine Esters to Generate (<italic toggle="yes">Z</italic>)-Tri- and Tetra-substituted Allylic Amino Acid Derivatives

Organic Letters
DOI: 10.1021/acs.orglett.0c01211




vinyl

Enhanced dielectric performance in flexible MWCNT/poly(vinylidene fluoride-co-hexafluoropropene)-based nanocomposites by designing a tri-layered structure

J. Mater. Chem. C, 2020, 8,5950-5957
DOI: 10.1039/D0TC00148A, Paper
Jie Chen, Yifei Wang, Jiufeng Dong, Yujuan Niu, Weixing Chen, Hong Wang
Tri-layered films are capable of excellent capacitive stability over straight bending (i.e. 20 000 cycles) and winding (i.e. 120 hours) tests.
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vinyl

[ASAP] Density and Thermodynamic Speed of Sound of Liquid Vinyl Chloride

Journal of Chemical & Engineering Data
DOI: 10.1021/acs.jced.9b01133




vinyl

Sequential C–O decarboxylative vinylation/C–H arylation of cyclic oxalates via a nickel-catalyzed multicomponent radical cascade

Chem. Sci., 2020, Advance Article
DOI: 10.1039/D0SC01471K, Edge Article
Open Access
  This article is licensed under a Creative Commons Attribution 3.0 Unported Licence.
Huan Li, Lei Guo, Xiaoliang Feng, Liping Huo, Shengqing Zhu, Lingling Chu
A selective, sequential C–O decarboxylative vinylation/C–H arylation of cyclic alcohol derivatives enabled by visible-light photoredox/nickel dual catalysis has been described.
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vinyl

Improving the determination of celecoxib in body fluids and pharmaceuticals using a new selective and thermosensitive molecularly imprinted poly(vinylidene fluoride) membrane

Anal. Methods, 2020, 12,2185-2195
DOI: 10.1039/D0AY00237B, Paper
Negin Yazdanian, Behrouz Akbari-Adergani, Maryam Kazemipour, Homayon Ahmad Panahi, Mehran Javanbakht
Molecularly imprinted membranes that demonstrated high selectivity for celecoxib were synthesized using N-vinylcaprolactam and 2-hydroxyethyl methacrylate.
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vinyl

Examining the vinyl moiety as a protecting group for hydroxyl (–OH) functionality under basic conditions

Org. Chem. Front., 2020, Advance Article
DOI: 10.1039/D0QO00202J, Research Article
Vladimir V. Voronin, Maria S. Ledovskaya, Konstantin S. Rodygin, Valentine P. Ananikov
A method for the protection and deprotection of alcohols via vinylation and devinylation reactions is proposed. Stability of the vinyl protecting group under various conditions is studied and synthetic applicability is demonstrated.
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vinyl

Organocatalytic 1,5-trifluoromethylthio-sulfonylation of vinylcyclopropane mediated by visible light in the water phase

Org. Chem. Front., 2020, Advance Article
DOI: 10.1039/D0QO00343C, Research Article
Junkai Liu, Hong Yao, Xinnan Li, Hongyu Wu, Aijun Lin, Hequan Yao, Jinyi Xu, Shengtao Xu
1,2-Difunctionalization has developed into a robust tool for the preparation of complex organic molecules, and remote difunctionalization has also aroused widespread interest to achieve pluripotency of difunctionalization.
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vinyl

Phosphine/Palladium Cooperative Catalysis: Enantioselective [5+4] Annulations of ortho-Quinone Methides and Vinylethylene Carbonates

Org. Chem. Front., 2020, Accepted Manuscript
DOI: 10.1039/D0QO00128G, Research Article
Chao Xia, Dong-Chao Wang, Gui-Rong Qu, Hai-Ming Guo
Highly enantioselective [5+4] annulations of ortho-quinone methides with vinylethylene carbonates were enabled by phosphine/palladium asymmetric cooperative catalysis for the first time. Efficient synthesis of various nine-membered benzo-heterocycles was achieved in...
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vinyl

Catalyst-Controlled Formal [4+1] Annulation of N-Vinyl Fluorenone Nitrones and Allenoates to Prepare Spirofluorenylpyrrolines

Org. Chem. Front., 2020, Accepted Manuscript
DOI: 10.1039/D0QO00224K, Research Article
Cui Wei, Jin-Qi Zhang, Jia-Jie Zhang, Cui Liang, Dong-Liang Mo
We report a readily commercial Gimeracil-catalyzed formal [4+1] annulation approach for the synthesis of spirofluorenylpyrrolines in good yields with high diastereoselectivity from easily available N-vinyl fluorenone nitrones and allenoates. The...
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vinyl

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...
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vinyl

[ASAP] Stereoselective Access to Highly Substituted Vinyl Ethers via <italic toggle="yes">trans</italic>-Difunctionalization of Alkynes with Alcohols and Iodine(III) Electrophile

Journal of the American Chemical Society
DOI: 10.1021/jacs.0c04140




vinyl

Constructing a tetraphenylethene (TPE) derivative-decorated polyvinyl alcohol (PVA)/lanthanide nanoparticle composite system for tunable luminescence

Dalton Trans., 2020, 49,5539-5546
DOI: 10.1039/D0DT00473A, Paper
Songyang Huang, Jianbin Wu, Jiale Li, Lirong Yu, Xi Wang, Ming Bai
It is found for the first time that TPEBA-modified PVA ligand-coated lanthanide nanoparticles display tunable luminescent properties due to the established energy transfer from the TPE-based ligand (donor) to the lanthanide nanoparticles (acceptor).
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vinyl

Chemoselective oxidative addition of vinyl sulfones mediated by palladium complexes bearing picolyl-N-heterocyclic carbene ligands.

Dalton Trans., 2020, 49,5684-5694
DOI: 10.1039/D0DT01144D, Paper
Thomas Scattolin, Claudio Santo, Nicola Demitri, Luciano Canovese, Fabiano Visentin
We have examined in depth the features of oxidative addition of (E)-1,2 ditosylethene on palladium(0) complexes bearing picolyl-N-heterocyclic carbenes.
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vinyl

[ASAP] Revealing the Dissolution Mechanism of Polyvinylidene Fluoride of Spent Lithium-Ion Batteries in Waste Oil-Based Methyl Ester Solvent

ACS Sustainable Chemistry & Engineering
DOI: 10.1021/acssuschemeng.0c02072




vinyl

The vinyl frontier: the story of the Voyager Golden Record / Jonathan Scott

Dewey Library - TL789.8.U6 V688 2019




vinyl

Synthesis of vinyl chloride monomer by acetylene hydrochlorination with a ruthenium-based N-heterocyclic carbene complex catalyst

Catal. Sci. Technol., 2020, Accepted Manuscript
DOI: 10.1039/D0CY00512F, Paper
Ming Cai, Haiyang Zhang, Baochang Man, Jian Li, Linfeng Li, Yanqin Li, Dongyang Xie, Renpan Deng, Jinli Zhang
With the implementation of Minamata Convention and the urgent demand for green, and efficient mercury-free catalysts, the carbon-supported IPr-(Ru)/AC catalyst was synthesized and assessed for its successful application in acetylene...
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vinyl

[ASAP] Expansion of Ovarian Cancer Stem-like Cells in Poly(ethylene glycol)-Cross-Linked Poly(methyl vinyl ether-<italic toggle="yes">alt</italic>-maleic acid) and Alginate Double-Network Hydrogels

ACS Biomaterials Science & Engineering
DOI: 10.1021/acsbiomaterials.9b01967




vinyl

[ASAP] Ultrathin Thin-Film Composite Polyamide Membranes Constructed on Hydrophilic Poly(vinyl alcohol) Decorated Support Toward Enhanced Nanofiltration Performance

Environmental Science & Technology
DOI: 10.1021/acs.est.9b06779




vinyl

Shintech will spend $1.5 billion to cement role as largest vinyl producer

The Louisiana project will complement an ethylene cracker the Japanese company is building in the state




vinyl

Vinyl cation busts some new moves

By tweaking its counter ion, classic carbocation inserts into C-H bonds




vinyl

[ASAP] [2 + 2] Cycloaddition of <italic toggle="yes">o</italic>-Carboryne with Vinyl Ethers: Synthesis of Carborane-Fused Cyclobutanes

Organometallics
DOI: 10.1021/acs.organomet.0c00163