Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Jierui Jing"'
Autor:
Yishou Wang, Xiaohan Zhu, Deng Pan, Jierui Jing, Fen Wang, Ruijie Mi, Genping Huang, Xingwei Li
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-12 (2023)
Abstract N-N axially chiral biaryls represent a rarely explored class of atropisomers. Reported herein is construction of diverse classes of diaxially chiral biaryls containing N-N and C-N/C-C diaxes in distal positions in excellent enantioselectivit
Externí odkaz:
https://doaj.org/article/82e8cd42f0984202a17fbfa7ad60e824
Publikováno v:
Chem. 8:3346-3362
Publikováno v:
Organic Letters. 24:2531-2535
Reported herein is the efficient and atroposelective construction of two categories of C-N atropisomers via rhodium(III)-catalyzed C-H activation of sulfoxonium ylides en route to [4+2] annulation with sterically hindered, electron-rich alkynes. This
Palladium-catalyzed atroposelective hydrophosphination of sterically hindered internal alkynes with secondary phosphines has been realized, affording C-N axially chiral trisubstituted olefins (vinylphosphines) in excellent regioselectivity, (E)-selec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76e01f10ef501a8e1ad565de15a0c3dc
https://doi.org/10.21203/rs.3.rs-1464877/v1
https://doi.org/10.21203/rs.3.rs-1464877/v1
Palladium-catalyzed unprecedented atroposelective hydrophosphination of internal alkynes has been realized using diarylphosphines, affording C-N axially chiral trisubstituted olefins (vinylphosphines) in excellent regioselectiviry, (E)-selectivity, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ae33011e609958b757223882d9c770b
https://doi.org/10.26434/chemrxiv-2021-8rtq4
https://doi.org/10.26434/chemrxiv-2021-8rtq4
Autor:
Yanliang Zhao, Liujie Zhao, Jierui Jing, Weiqiao Deng, Xue-Peng Zhang, Panjie Hu, Fen Wang, Xiaohan Zhu, Xingwei Li
Publikováno v:
Angewandte Chemie (International ed. in English). 60(30)
Reported herein is asymmetric [3+2] annulation of arylnitrones with different classes of alkynes catalyzed by chiral rhodium(III) complexes, with the nitrone acting as an electrophilic directing group. Three classes of chiral indenes/indenones have b
Autor:
Jierui Jing, Xingwei Li, Xujing Duan, Shuailei Zhai, Jiaqiong Sun, Xiaojiao Li, Guangfan Zheng, Lu Chen
Publikováno v:
The Journal of organic chemistry. 85(6)
Reported herein is the Rh(III)-catalyzed annulation of N-unprotected 2-arylindoles with quinone monoacetals for the straightforward synthesis of [4,3,1]-bridged carbocycles with exclusive C(3) selectivity. Mechanistic studies, particularly deuterium-