Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Zheng‐Xin Zhou"'
Autor:
Yu‐Qing Xiao, Miao‐Miao Li, Zheng‐Xin Zhou, Yu‐Jie Li, Meng‐Yue Cao, Xiao‐Peng Liu, Hai‐Hua Lu, Li Rao, Liang‐Qiu Lu, André M. Beauchemin, Wen‐Jing Xiao
Publikováno v:
Angewandte Chemie (International ed. in English). 62(3)
Ring-opening transformations of donor-acceptor (D-A) cyclopropanes enable the rapid assembly of complex molecules. However, the enantioselective formation of chiral quaternary stereocenters using substrates bearing two different acceptors remains a c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31ffbec8cb78a325fe6a06c73096822b
https://pubmed.ncbi.nlm.nih.gov/36377924
https://pubmed.ncbi.nlm.nih.gov/36377924
Publikováno v:
Organic Letters. 23:2057-2062
Herein, we disclose a ruthenium-catalyzed meta-selective C-H activation of phosphines by using intrinsic P(III) as a directing group. 2,2,6,6-Tetramethylheptane-3,5-dione acts as the ligand and exhibits an excellent performance in boosting the meta-a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0a7fd6d125606861b2d27eb0d6d3f5c
https://doi.org/10.1021/acs.orglett.1c00237
https://doi.org/10.1021/acs.orglett.1c00237
Autor:
Ming-Hua Zeng, Mohamedally Kurmoo, Yue-Jin Liu, Rou-Ming Peng, Pan-Ting Tang, Yi Wei, Jia-Wei Li, Xiao-Peng Luo, Zheng-Xin Zhou, Abing Duan
Publikováno v:
Organic Letters. 22:4129-4134
Biphenylcarboxylic acid with two competing C(sp2)-H sites was designed for site selective C(sp2)-H functionalization by developing carboxylic acids assisted remote and selective olefination via 7-membered palladacycle. Mechanism investigation and DFT
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e01368ee338f8bbb99d4aa624f68b035
https://doi.org/10.1021/acs.orglett.0c01208
https://doi.org/10.1021/acs.orglett.0c01208
Publikováno v:
Journal of Hainan Medical University; Feb2023, Vol. 29 Issue 4, p38-45, 8p
Autor:
Yue-Jin Liu, Cui-Hong Chen, Zheng-Xin Zhou, Wei-Hao Rao, Bin Liu, Yun Chai, Ming-Hua Zeng, Li Liu, Ran Xu
Publikováno v:
Organic Chemistry Frontiers. 6:442-446
Ligand-promoted room-temperature Pd(II)-catalyzed direct C–H alkynylation of phenylacetic amides has been developed using commercially available TIPS-acetylene as an efficient alkynylating reagent, where 8-aminoquinoline was employed as a removable
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a5791221ea65b485efc58b63604c398
https://doi.org/10.1039/c8qo01215f
https://doi.org/10.1039/c8qo01215f
Autor:
Cai-yu, ZHU, Zheng-xin, ZHOU, Yi-fan, GU, Shi-ding, HAN, Huan, XU, Zhuang-zhuang, WANG, Lei, ZHU
Publikováno v:
Journal of Hainan Medical University; Oct2022, Vol. 28 Issue 20, p11-17, 7p
Publikováno v:
Organic letters. 23(6)
Herein, we disclose a ruthenium-catalyzed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cd3b2b061b0fdc787d568535acfbd07f
https://pubmed.ncbi.nlm.nih.gov/33630602
https://pubmed.ncbi.nlm.nih.gov/33630602
Autor:
Yi, Wei, Abing, Duan, Pan-Ting, Tang, Jia-Wei, Li, Rou-Ming, Peng, Zheng-Xin, Zhou, Xiao-Peng, Luo, Mohamedally, Kurmoo, Yue-Jin, Liu, Ming-Hua, Zeng
Publikováno v:
Organic letters. 22(11)
Biphenylcarboxylic acid with two competing C(sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e99fad276051353855dc9a19e207119a
https://pubmed.ncbi.nlm.nih.gov/32459099
https://pubmed.ncbi.nlm.nih.gov/32459099
Publikováno v:
Organic Letters. 20:7274-7277
A weakly carboxylate-directed palladium(II)-catalyzed ortho-C-H alkynylation of diverse phenylacetic acids promoted by monoprotected amino acid ligand enabled is reported. The reaction has a broad substrate scope including α-secondary, tertiary, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::458dc72438526fa5dfde15dd8db60534
https://doi.org/10.1021/acs.orglett.8b03182
https://doi.org/10.1021/acs.orglett.8b03182
Publikováno v:
Chemical Communications. 54:14136-14139
Pd(II)-Catalyzed direct C(sp3)–H germylation of α-AA derivatives with the assistance of a bidentate auxiliary for the efficient synthesis of β-germyl-α-amino amides is reported. This protocol features good generality for primary and secondary C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f201b4d099ad2bff1f96a06e92fbe185
https://doi.org/10.1039/c8cc08098d
https://doi.org/10.1039/c8cc08098d