16 Jan 08:16
Green Chem., 2024, 26,2692-2704
DOI: 10.1039/D3GC04400A, Paper
Hyungjoo Kim, Yong Hyun Lim, Jae Hyun Park, Jeong-Myeong Ha, Do Heui Kim
The physically mixed Co/TiO2 and WO3/TiO2 catalysts exhibited excellent catalytic performance in the hydrodeoxygenation of guaiacol, and the deactivated catalyst could be successfully regenerated after magnetic separation.
The content of this RSS Feed (c) The Royal Society of Chemistry
15 Jan 16:23
by Sara Bonfante, Christian Lorber, Jason M. Lynam, Antoine Simonneau, and John M. Slattery

Journal of the American Chemical Society
DOI: 10.1021/jacs.3c10614
15 Jan 16:18
Green Chem., 2024, 26,1846-1875
DOI: 10.1039/D3GC04154A, Tutorial Review
Quanbin Jiang, Jie Luo, Xiaodan Zhao
Organocatalytic enantioselective cross-dehydrogenative coupling reaction provides a great opportunity for the synthesis of highly enantioenriched molecules. In this review, recent progress in this field is summarized.
The content of this RSS Feed (c) The Royal Society of Chemistry
15 Jan 07:57
by Robin Van Echelpoel
Nature Reviews Chemistry, Published online: 12 January 2024; doi:10.1038/s41570-023-00571-1
The European BorderSens project leverages voltammetric sensors, developed with end-users’ input, to rapidly and accurately detect illicit drugs. By embracing practicalities and validation, this technology has the potential to combat the illicit drug problem.
12 Jan 15:53
by Kai Wu, Bingbing Luo, Ke Yang, Siyu Wang, Mingfan Li, and Huiyan Zhang

ACS Sustainable Chemistry & Engineering
DOI: 10.1021/acssuschemeng.3c06294
08 Jan 08:00
by Linhao Zhong, Xiaoqing Liao, Haishuai Cui, He’an Luo, Yang Lv, and Pingle Liu

ACS Catalysis
DOI: 10.1021/acscatal.3c03624
08 Jan 07:58
by Gang Sun, Shi-Ping Zhan, Yi-Feng Zhao, Xingyi Du, Mao-Ying Shi, Jing Li, Haoliang Yuan, Xiaoan Wen, Hongbin Sun, and Qing-Long Xu

The Journal of Organic Chemistry
DOI: 10.1021/acs.joc.3c02175
08 Jan 07:54
by Jin-Xuan Xie, Yun-Peng Zhao, Qiang Li, Le-Le Qiu, Fang-Jing Liu, Jing Liang, Jian Li, and Jing-Pei Cao

ACS Sustainable Chemistry & Engineering
DOI: 10.1021/acssuschemeng.3c05931
08 Jan 07:54
by Zhibing Chen, Saisai Wang, Jia Zhao, and Ronghe Lin

ACS Catalysis
DOI: 10.1021/acscatal.3c04495
08 Jan 07:51
by Sergio Parra-García, Marina Ballester-Ibáñez, and José-Antonio García-López

The Journal of Organic Chemistry
DOI: 10.1021/acs.joc.3c01750
08 Jan 07:46
by Ben. J. Tickner, Marcus Dennington, Benjamin G. Collins, Callum A. Gater, Theo F. N. Tanner, Adrian C. Whitwood, Peter J. Rayner, Daniel P. Watts, and Simon B. Duckett

ACS Catalysis
DOI: 10.1021/acscatal.3c05378
08 Jan 07:46
by Heungjin Ryu

We report seasonal and individual variations in urinary creatinine levels in Eastern Bent-winged Bats in Korea. Our findings suggest a link between water stress and winter arousal, as well as an influence of the surface-to-volume ratio on urinary creatinine levels.
08 Jan 07:45
by Zhenya Zhang, Bolong Li, Jianghao Wang, Jing Li, and Jie Fu

ACS Sustainable Chemistry & Engineering
DOI: 10.1021/acssuschemeng.3c06906
08 Jan 07:42
by Max Kozlov
Nature, Published online: 05 January 2024; doi:10.1038/d41586-024-00012-z
Military veterans with cognitive and psychological problems saw drastic improvements after a dose of ibogaine.
04 Jan 16:08
Chem. Commun., 2024, 60,1043-1046
DOI: 10.1039/D3CC04282K, Communication

Open Access
Marie-Hélène Pietraru, Louise Ponsard, Nicolas Lentz, Pierre Thuéry, Emmanuel Nicolas, Thibault Cantat
We describe the synthesis, characterisation, and use as carbonylation catalysts of four organic Lewis acids based on fluorophosphoniums, with tetracarbonyl cobaltate as the counter-anion: [R3PF]+[Co(CO)4]− (with R = o-Tol, Cy, iPr, and tBu).
The content of this RSS Feed (c) The Royal Society of Chemistry
04 Jan 15:18
by Amit , Kumar
We report here a new method to make polyketones from the coupling of diketones and diols using a manganese pincer complex. The methodology allows us to access a new type of polyketone (polyarylalkylketone) containing aryl, alkyl, and ether functionalities bridging the gap between the two classes of commercially available polyketones – aliphatic polyketones and polyaryletherketones. Using this methodology, twelve new polyketones have been synthesized and characterised using various analytical techniques to understand their chemical, physical, morphological, and mechanical properties. Based on previous reports and our studies, we suggest that the polymerization occurs via a hydrogen-borrowing mechanism that involves the dehydrogenation of diols to dialdehyde followed by aldol condensation of dialdehyde with diketones to form chalcone derivatives and their subsequent hydrogenation to form polyarylalkylketones.
04 Jan 14:51
by Bo Xiang, Peng Xu, Renzhi Li, and Rong Zhang

ACS Sustainable Chemistry & Engineering
DOI: 10.1021/acssuschemeng.3c05583
02 Jan 08:27
by Matías Horst, Jan Meisner, Jinghui Yang, Tatiana B. Kouznetsova, Stephen L. Craig, Todd J. Martínez, and Yan Xia

Journal of the American Chemical Society
DOI: 10.1021/jacs.3c11293
02 Jan 08:26
by Dehui Kong, Tyler Fahrenhorst-Jones, Andy Kuo, Jacinta L. Simmons, Lendl Tan, Jed M. Burns, Gregory K. Pierens, Rui Li, Nicholas P. West, Glen M. Boyle, Maree T. Smith, G. Paul Savage, and Craig M. Williams

The Journal of Organic Chemistry
DOI: 10.1021/acs.joc.3c02333
02 Jan 08:24
by Umair Akram

While mental health memes typically depict dark and negative humour, their proximal nature to those
experiencing psychiatric symptoms may be considered contextually positive. Our work evaluates the potential of internet memes as a coping mechanism for those experiencing psychiatric distress.
02 Jan 08:23
by Arnaud Olivier and Daniel S. Müller

Organic Process Research & Development
DOI: 10.1021/acs.oprd.3c00418
02 Jan 08:22
by Congjian Xia, Haiyang Hu, Wengang Xu, Baokai Yang, Qi Shao, and Mingbo Wu

Organic Letters
DOI: 10.1021/acs.orglett.3c03982
02 Jan 08:14
by Wilson C. Edenfield, Alexander H. Mason, Qingheng Lai, Amol Agarwal, Takeshi Kobayashi, Yosi Kratish, and Tobin J. Marks

ACS Catalysis
DOI: 10.1021/acscatal.3c05161
02 Jan 08:06
by Zhong Li, Yunwei Huang, Haoyang Li, Fenghua Zhang, Yazhou Ren, Wenxiong Shi, Qingda Liu, and Xun Wang

Journal of the American Chemical Society
DOI: 10.1021/jacs.3c09752
02 Jan 08:04
by Carlota Odena, Enrique Gómez-Bengoa, and Ruben Martin

Journal of the American Chemical Society
DOI: 10.1021/jacs.3c12497
02 Jan 08:00
by Amin Ghaderikia and Yasemin Dilsad Yilmazel

ACS Sustainable Chemistry & Engineering
DOI: 10.1021/acssuschemeng.3c05370
02 Jan 07:59
by Ramesh Goura, Surendra Babu Manabolu Surya, Naresh Kumar Katari, Ramprasad Achampeta Kodanda, Pradeep Rebelly, and Nagaraju Chakilam

Organic Process Research & Development
DOI: 10.1021/acs.oprd.3c00313
02 Jan 07:57
by Maoping Pu, Christian D.-T. Nielsen, Erdem Senol, Theresa Sperger, and Franziska Schoenebeck

JACS Au
DOI: 10.1021/jacsau.3c00724
02 Jan 07:54
by Linzi Wen, Ziyan Zou, Naifu Zhou, Chengbo Sun, Peixu Xie, and Pengju Feng

Organic Letters
DOI: 10.1021/acs.orglett.3c03901