Zobrazeno 1 - 10
of 820
pro vyhledávání: '"Teck-Peng Loh"'
Publikováno v:
Advanced Science, Vol 11, Iss 31, Pp n/a-n/a (2024)
Abstract In this study, a novel approach for the tertiary α‐alkylation of ketones using alkanes with electron‐deficient C─H bonds is presented, employing a synergistic catalytic system combining inexpensive copper salts with aminocatalysis. Th
Externí odkaz:
https://doaj.org/article/85d3fe1dd26b49ee9161e0c755e39f76
Publikováno v:
Green Synthesis and Catalysis, Vol 3, Iss 4, Pp 309-316 (2022)
Methods for the carbon-sulfur bond formation under catalyst-free, aqueous conditions are extremely useful in organic synthesis and chemical biology. Our laboratory has developed methodologies to construct carbon-thiol bonds, carbon-sulfinic acid bond
Externí odkaz:
https://doaj.org/article/7c2d35f4f82f404ab751bbfbd475b9c0
Autor:
Peizhong Xie, Jinyu Wang, Yanan Liu, Jing Fan, Xiangyang Wo, Weishan Fu, Zuolian Sun, Teck-Peng Loh
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-8 (2018)
Despite the biological importance of sulfones, available synthetic methods usually involve toxic metals and reagents or harsh conditions. Here, the authors report an environmentally benign procedure for the metal-free carbon-sulfur bond formation of
Externí odkaz:
https://doaj.org/article/c0831286fa2a4e238e31d29f3298ec4a
Autor:
Cheng Bao, Xia Liu, Meng Li, Jing Meng, Yongliang Cai, Xiao Huang, Teck-Peng Loh, Zhijuan Wang
Publikováno v:
Electrochemistry Communications, Vol 106, Iss , Pp - (2019)
A MoS2-nanosheet-decorated C-N/Co4S3 (C-N/Co4S3@MoS2) nanorod with multi-defects was synthesized by using a core-shell zeolitic imidazole framework (ZIF-8@ZIF-67) as the precursor. The C-N/Co4S3@MoS2 hybrid showed high activity towards the hydrogen e
Externí odkaz:
https://doaj.org/article/17371059d2d440a2832a2a057da09ed9
Publikováno v:
Molecules, Vol 23, Iss 4, p 979 (2018)
A combined Lewis acid system comprising of two or more Lewis acids occasionally exhibits augmented catalytic activity in organic transformations which are otherwise unrealizable by either of the components exclusively. On the other hand, the efficien
Externí odkaz:
https://doaj.org/article/47df67d074b246dcb26ce58093ea5ed5
Autor:
Xiaotong Fan, Siqi Liu, Zhenhua Jia, J. Justin Koh, Jayven Chee Chuan Yeo, Chen-Gang Wang, Nayli Erdeanna Surat'man, Xian Jun Loh, Jean Le Bideau, Chaobin He, Zibiao Li, Teck-Peng Loh
Publikováno v:
Chemical Society Reviews. 52:2497-2527
This review describes the most recent developments in materials design and the advanced features of ionogels, as well as their emerging biomedical applications.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ee1fe74e1ef3f30cc6974dc464a23bd
https://doi.org/10.1039/d2cs00652a
https://doi.org/10.1039/d2cs00652a
Publikováno v:
Chemical Communications. 59:223-226
A metal-free strategy regarding iodine catalysis to achieve ortho-aminomethylation of phenols in aqueous media has been developed, which is highlighted by the late-stage functionalization of drug molecules containing phenolic structures.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be2ad6b0db7591ce46e5141328efccd0
https://doi.org/10.1039/d2cc05746h
https://doi.org/10.1039/d2cc05746h
Publikováno v:
Organic Letters. 24:9355-9360
A Pd/Ca catalytic system to promote the unsymmetrical bis-allylation of malononitrile was developed by selecting conjugated dienes and allylic alcohols as allylic reagents. This catalytic system suppressed the competitive symmetrical bis-allylation p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8ad2146af6a79985592a58d3b73e6e9
https://doi.org/10.1021/acs.orglett.2c03405
https://doi.org/10.1021/acs.orglett.2c03405
Autor:
Zhenguo Zhang, Jun Gu, Liang Ji, Xiaoxiao Liu, Ting Zhang, Yongheng Lv, Fang Liu, Zhenhua Jia, Teck-Peng Loh
Publikováno v:
ACS Catalysis. 12:14123-14129
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3ac2aa76eccb98794cf907532ff6d6d1
https://doi.org/10.1021/acscatal.2c04010
https://doi.org/10.1021/acscatal.2c04010
Publikováno v:
Chemical Reviews. 122:17479-17646
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ff9ff3151d2d306c106bd543b396e0c
https://doi.org/10.1021/acs.chemrev.2c00032
https://doi.org/10.1021/acs.chemrev.2c00032