no

[ASAP] Soft Polymeric Matrix as a Macroscopic Cage for Magnetically Modulating Reversible Nanoscale Ligand Presentation

Nano Letters
DOI: 10.1021/acs.nanolett.9b05315




no

[ASAP] Ultrasmall Rhodium Nanozyme with RONS Scavenging and Photothermal Activities for Anti-Inflammation and Antitumor Theranostics of Colon Diseases

Nano Letters
DOI: 10.1021/acs.nanolett.9b05035




no

[ASAP] Multimodal Enzyme Delivery and Therapy Enabled by Cell Membrane-Coated Metal–Organic Framework Nanoparticles

Nano Letters
DOI: 10.1021/acs.nanolett.0c01654




no

[ASAP] Reduction of Optical Gain Threshold in CsPbI<sub>3</sub> Nanocrystals Achieved by Generation of Asymmetric Hot-Biexcitons

Nano Letters
DOI: 10.1021/acs.nanolett.0c01079




no

[ASAP] A Nanoprimer To Improve the Systemic Delivery of siRNA and mRNA

Nano Letters
DOI: 10.1021/acs.nanolett.0c00752




no

[ASAP] Core–Shell Tunnel Junction Nanowire White-Light-Emitting Diode

Nano Letters
DOI: 10.1021/acs.nanolett.0c00420




no

[ASAP] In Liquid Infrared Scattering Scanning Near-Field Optical Microscopy for Chemical and Biological Nanoimaging

Nano Letters
DOI: 10.1021/acs.nanolett.0c01291




no

[ASAP] Bi–Sn Catalytic Foam Governed by Nanometallurgy of Liquid Metals

Nano Letters
DOI: 10.1021/acs.nanolett.0c01170




no

[ASAP] Core–Shell C@Sb Nanoparticles as a Nucleation Layer for High-Performance Sodium Metal Anodes

Nano Letters
DOI: 10.1021/acs.nanolett.0c01257




no

[ASAP] Propagation of Spin-Wave Packets in Individual Nanosized Yttrium Iron Garnet Magnonic Conduits

Nano Letters
DOI: 10.1021/acs.nanolett.0c00657




no

[ASAP] Stretchable Nanolayered Thermoelectric Energy Harvester on Complex and Dynamic Surfaces

Nano Letters
DOI: 10.1021/acs.nanolett.0c01225




no

[ASAP] Simultaneous Intravital Optical and Acoustic Monitoring of Ultrasound-Triggered Nanobubble Generation and Extravasation

Nano Letters
DOI: 10.1021/acs.nanolett.0c01310




no

Economic incentives for marine and coastal conservation : prospects, challenges and policy implications / edited by Essam Yassin Mohammed




no

Marine pollution : what everyone needs to know / Judith S. Weis

Weis, Judith S., 1941-




no

Ocean waves and kindred geophysical phenomena / by Vaughan Cornish with photographs by the author and additional notes by Harold Jeffreys

Cornish, Vaughan, 1862-1948




no

Invitation to oceanography / Paul R. Pinet

Pinet, Paul R




no

Marine genomics : methods and protocols / edited by Sarah J. Bourlat, Department of Marine Sciences, University of Gothenburg, Gothenburg, Sweden




no

Introduction to physical oceanography / John A. Knauss (late of University of Rhode Island), Newell Garfield (Southwest Fisheries Science Center)

Knauss, John A., author




no

Marine community ecology and conservation / edited by Mark D. Bertness, Brown University, John F. Bruno, University of North Carolina, Chapel Hill, Brian R. Silliman, Duke University, John J. Stachowicz, University of California Davis

Bertness, Mark D., 1949-




no

Economics of the marine : modelling natural resources / Karyn Morrissey

Morrissey, Karyn, author




no

Marine plankton : a practical guide to ecology, methodology and taxonomy / edited by Claudia Castellani (Sir Alister Hardy Foundation for Ocean Science, Plymouth, UK) and Martin Edwards (Sir Alister Hardy Foundation for Ocean Science, Plymouth, UK and Uni




no

Environmental governance reconsidered : challenges, choices, and opportunities / edited by Robert F. Durant, Daniel J. Fiorino, and Rosemary O'Leary




no

Marine conservation / P. Keith Probert (Department of Marine Science, University of Otago) ; with an initial contribution by the late Norman A. Holme

Probert, P. Keith, author




no

The water-food-energy nexus : processes, technologies, and challenges / edited by I.M. Mujtaba, R. Srinivasan, N.O. Elbashir




no

Environmental security in the anthropocene : assessing theory and practice / Judith Nora Hardt

Hardt, Judith Nora, author




no

Essentials of oceanography / Alan P. Trujillo (Distinguished Teaching Professor, Palomar College), Harold V. Thurman (Former Professor Emeritus, MT. San Antonio College)

Trujillo, Alan P., author




no

Fundamentals of estuarine physical oceanography / Luiz Bruner de Miranda, Fernando Pinheiro Andutta, Björn Kjerfve, Belmiro Mendes de Castro Filho

Miranda, Luiz Bruner de, author




no

Investigating oceanography / Keith A. Sverdrup (University of Wisconsin-Milwaukee), Raphael M. Kudela (University of California, Santa Cruz)

Sverdrup, Keith A., author




no

Evolutionary ecology of marine invertebrate larvae / edited by Tyler J. Carrier (University of North Carolina at Charlotte, USA), Adam M. Reitzel (University of North Carolina at Charlotte, USA), Andreas Heyland (University of Guelph, Canada)




no

Microplastics in fisheries and aquaculture : status of knowledge on their occurrence and implications for aquatic organisms and food safety / Amy Lusher, Peter Hollman, and Jeremy Mendoza-Hill

Lusher, Amy, author




no

Coastal management : global challenges and innovations / edited by R.R. Krishnamurthy, M.P. Jonathan, Seshachalam Srinivasalu, Bernhard Glaeser




no

Freshwater ecology : concepts and environmental applications of limnology / Walter K. Dodds, Matt R. Whiles

Dodds, Walter K. (Walter Kennedy), 1958- author




no

Essentials of oceanography / Alan P. Trujillo (Distinquished Teaching Professional, Palomar College), Harold V. Thurman (Former Professor Emeritus, Mt. San Antonio College)

Trujillo, Alan P., author




no

Leveraging Wikipedia: connecting communities of knowledge / edited by Merrilee Proffitt

Barker Library - Z674.75.W55 L48 2018




no

Palladium-catalyzed synthesis of [60]fullerene-fused furochromenones and further electrochemical functionalization

Org. Chem. Front., 2020, Advance Article
DOI: 10.1039/D0QO00264J, Research Article
Majid Hussain, Chuang Niu, Guan-Wu Wang
The palladium-catalyzed heteroannulation of [60]fullerene with 4-hydroxycoumarins affords [60]fullerene-fused furochromenones, which can be further derivatized via an electrochemical method to synthesize 1,2,3,4-adducts.
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no

Rhodium-catalyzed asymmetric transfer hydrogenation of 4-quinolone derivatives

Org. Chem. Front., 2020, 7,975-979
DOI: 10.1039/C9QO01514K, Research Article
Bin He, Phannarath Phansavath, Virginie Ratovelomanana-Vidal
4-Quinolone derivatives were conveniently reduced to 1,2,3,4-tetrahydroquinoline-4-ols with excellent enantioselectivities through asymmetric transfer hydrogenation using a tethered rhodium complex and formic acid/triethylamine as the hydride source.
The content of this RSS Feed (c) The Royal Society of Chemistry




no

Copper-catalyzed tandem phosphorylative allenylation/cyclization of 1-(o-aminophenyl)prop-2-ynols with the P(O)–H species: access to C2-phosphorylmethylindoles

Org. Chem. Front., 2020, 7,980-986
DOI: 10.1039/D0QO00159G, Research Article
Xiao-Yan Liu, Yun-Xiang Zou, Hai-Liang Ni, Jing Zhang, Hong-Bo Dong, Long Chen
A novel method to synthesize C2-phosphorylmethylindoles via the carbocation formation initiated tandem phosphorylative allenylation/cyclization of 1-(o-aminophenyl)prop-2-ynols with the P(O)–H species has been developed.
The content of this RSS Feed (c) The Royal Society of Chemistry




no

Total synthesis of tumor-associated KH-1 antigen core nonasaccharide via photo-induced glycosylation

Org. Chem. Front., 2020, Advance Article
DOI: 10.1039/D0QO00314J, Research Article
Bo-Han Li, Wenlong Yao, Hong Yang, Congying Wu, De-Cai Xiong, Yuxin Yin, Xin-Shan Ye
KH-1 antigen core nonasaccharide was efficiently assembled by photo-induced glycosylation.
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The content of this RSS Feed (c) The Royal Society of Chemistry




no

Folding of fluorinated oligoarylenes into non-alternant PAHs with various topological shapes

Org. Chem. Front., 2020, Advance Article
DOI: 10.1039/D0QO00370K, Research Article
Vladimir Akhmetov, Andreas Förtsch, Mikhail Feofanov, Sergey Troyanov, Konstantin Amsharov
An unprecedented [6]helicene's cavity closure indicating the possibility of introducing seven-membered rings via alumina-mediated C–F activation is shown.
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The content of this RSS Feed (c) The Royal Society of Chemistry




no

Rh-Catalyzed nitrene alkyne metathesis/formal C–N bond insertion cascade: synthesis of 3-iminoindolines

Org. Chem. Front., 2020, Advance Article
DOI: 10.1039/D0QO00294A, Research Article
Kemiao Hong, Su Zhou, Wenhao Hu, Xinfang Xu
A Rh-catalyzed nitrene/alkyne metathesis (NAM) cascade reaction terminated by a formal C–N bond insertion has been developed, which provides facile access to the tricyclic 3-iminoindolines in good yields with broad substrate scope.
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The content of this RSS Feed (c) The Royal Society of Chemistry




no

Access to SCN-containing thiazolines via electrochemical regioselective thiocyanothiocyclization of N-allylthioamides

Org. Chem. Front., 2020, Advance Article
DOI: 10.1039/D0QO00300J, Research Article
Yan-An Zhang, Zhong Ding, Peng Liu, Wei-Si Guo, Li-Rong Wen, Ming Li
An electrochemical thiocyclization of N-allylthioamides has been developed for the synthesis of SCN-containing 2-thiazolines and NCS-containing thiazines.
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The content of this RSS Feed (c) The Royal Society of Chemistry




no

Discovery of new polycyclic polyprenylated acylphloroglucinols with diverse architectures as potent cyclooxygenase-2 inhibitors

Org. Chem. Front., 2020, Advance Article
DOI: 10.1039/D0QO00259C, Research Article
Shuangshuang Xie, Changxing Qi, Yulin Duan, Qianqian Xu, Yaping Liu, Yingying Huang, Xu Yin, Weiguang Sun, Yuan Zhou, Yonghui Zhang
Cyclooxygenase-2 (COX-2) is a significant therapeutic target of chronic inflammatory diseases.
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The content of this RSS Feed (c) The Royal Society of Chemistry




no

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.
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The content of this RSS Feed (c) The Royal Society of Chemistry




no

Roquefornine A, a sesterterpenoid with a 5/6/5/5/6-fused ring system from the fungus Penicillium roqueforti YJ-14

Org. Chem. Front., 2020, Accepted Manuscript
DOI: 10.1039/D0QO00301H, Research Article
Jia-Peng Wang, Yan Shu, Jun-Tao Hu, Rui Liu, Xue-Yun Cai, Cheng-Tong Sun, Dong Gan, Di-Jiao Zhou, Rui-Feng Mei, Hao Ding, Xiao-Ran Zhang, Le Cai, Zhong-Tao Ding
Roquefornine A, a sesterterpenoid with an unprecedented 5/6/5/5/6-membered pentacyclic system, was characterized from Penicillium roqueforti YJ-14. Its structure was determined by extensive spectroscopic analyses, [Rh2(OCOCF3)4]-induced CD data and DP4+ calculations....
The content of this RSS Feed (c) The Royal Society of Chemistry




no

Asymmetric Organocatalytic Double 1,6-Addition: Rapid Access to Chiral Chromans with Molecular Complexity

Org. Chem. Front., 2020, Accepted Manuscript
DOI: 10.1039/D0QO00354A, Research Article
Indranil Chatterjee, Sourav Roy, Suman Pradhan, Krishan Kumar
An organocatalytic cascade vinylogous double 1,6-addition strategy for the synthesis of chiral chroman derivatives is reported. The cascade reaction follows oxa-Michael/1,6-addition reactions between ortho-hydroxyphenyl-substituted para-quinone methadies and 2,4-dienal derivatives to...
The content of this RSS Feed (c) The Royal Society of Chemistry




no

Access to cyano-substituted pyrazolines through copper-catalyzed cascade cyanation/cyclization of unactivated olefins

Org. Chem. Front., 2020, Advance Article
DOI: 10.1039/D0QO00282H, Research Article
Fei Meng, Qin Fang, Weidong Yuan, Ning Xu, Shujun Cao, Jianlin Chun, Jie Li, Honglin Zhang, Yingguang Zhu
A mild copper-catalyzed cascade cyanation/cyclization of hydrazone-tethered unactivated olefins was developed for the efficient and practical synthesis of cyano-containing pyrazolines.
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no

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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no

Hyperforones A–C, benzoyl-migrated [5.3.1]-type polycyclic polyprenylated acylphloroglucinols from Hypericum forrestii

Org. Chem. Front., 2020, 7,1070-1076
DOI: 10.1039/D0QO00152J, Research Article
Wei-Jia Lu, Wen-Jun Xu, Yan-Qiu Zhang, Yi-Ran Li, Xin Zhou, Qi-Ji Li, Hao Zhang, Jun Luo, Ling-Yi Kong
Unprecedented benzoyl-migrated polycyclic polyprenylated acylphloroglucinols with a unique C-1 H-substituted bicyclo[5.3.1]hendecane framework, hyperforones A–C (1–3), were isolated from Hypericum forrestii.
The content of this RSS Feed (c) The Royal Society of Chemistry




no

Differential formation of nitrogen-centered radicals leading to unprecedented, regioselective bromination of N,N'-(1,2-phenylene)bisamides and 2-amidophenols

Org. Chem. Front., 2020, 7,1095-1106
DOI: 10.1039/C9QO01508F, Research Article
Damoder Reddy Motati, Dilipkumar Uredi, Amarender Goud Burra, J. Phillip Bowen, Frank R. Fronczek, Clint R. Smith, E. Blake Watkins
A highly efficient, site-selective, visible light-accelerated, remote C–H halogenation of unsymmetrical aromatic bisamides/amidoesters has been developed.
The content of this RSS Feed (c) The Royal Society of Chemistry




no

Toward C2-nitrogenated chromones by copper-catalyzed β-C(sp2)–H N-heteroarylation of enaminones

Org. Chem. Front., 2020, 7,1107-1112
DOI: 10.1039/D0QO00065E, Research Article
Tian Luo, Jie-Ping Wan, Yunyun Liu
The synthesis of C2-nitrogenated chromones has been performed via reactions of enaminones and nitrogen nucleophiles based on an unconventional β-C–H bond functionalization and a featured chromone annulation of enaminones.
The content of this RSS Feed (c) The Royal Society of Chemistry