Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Wen-Xin Fan"'
Autor:
Yin Li, Wen-Xin Fan, Shuang Luo, Alina Trofimova, Yuan Liu, Jiang-Hao Xue, Ling Yang, Qingjiang Li, Honggen Wang, Andrei K. Yudin
Publikováno v:
Journal of the American Chemical Society. 145:7548-7558
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce58ce93749200d720fcfa545a9857a1
https://doi.org/10.1021/jacs.3c00860
https://doi.org/10.1021/jacs.3c00860
Autor:
Wen-Xin Fan, Honggen Wang, Jia-Qiang Wu, Zhi-Shu Huang, Dong-Hang Tan, Xu-Ge Liu, Qingjiang Li, Ling Yang
Publikováno v:
Angewandte Chemie International Edition. 60:3454-3458
α-Haloboronates are useful organic synthons that can be converted to a diverse array of α-substituted alkyl borons. Methods to α-haloboronates are limiting and often suffer from harsh reaction conditions. Reported herein is a photochemical radical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d4ce2b675a8a8b4d26a768d41f1c178
https://doi.org/10.1002/anie.202011872
https://doi.org/10.1002/anie.202011872
Publikováno v:
Chemical Communications. 56:82-85
The iodofluorination of alkynyl and alkenyl MIDA (N-methyliminodiacetyl) boronates led to the synthesis of two types of fluorinated organoborons bearing a valuable C-I bond. The B(MIDA) moiety confers exclusive regioselectivity to the reaction, and t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21c331c7f9fec26a7b32644936dd47df
https://doi.org/10.1039/c9cc08386c
https://doi.org/10.1039/c9cc08386c
Publikováno v:
Chemical science. 13(21)
The selenium-π-acid-catalysis has received increasing attention as a powerful tool for olefin functionalization, but the regioselectivity is often problematic. Reported herein is a selenium-catalyzed regiocontrolled olefin transpositional chlorinati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::58851027badd3e95ed41bc33e963e009
https://pubmed.ncbi.nlm.nih.gov/35733886
https://pubmed.ncbi.nlm.nih.gov/35733886
The selenium-pi-acid-catalysis has received increasing attention as powerful tools for olefin functionalization, but the regioselectivity is often problematic. Reported herein is a selenium-catalyzed regiocontrolled olefin transpositional chlorinatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5564a4193b999018431be21c91fe8591
https://doi.org/10.26434/chemrxiv-2021-0lw7k
https://doi.org/10.26434/chemrxiv-2021-0lw7k
Publikováno v:
Chemical communications (Cambridge, England). 56(31)
The synthesis of α-boryl halohydrins via difunctionalization of alkenyl MIDA boronates has been reported. Intriguing stereoselectivity was found with different halogen sources, which arises from the special stabilizing effect of the B(MIDA) moiety.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9682b7f44e568f24d2f8cc79c61c6b6
https://pubmed.ncbi.nlm.nih.gov/32191245
https://pubmed.ncbi.nlm.nih.gov/32191245
Autor:
Qingjiang Li, E Lin, Zhan Li, Honggen Wang, Yuan-Hong Cai, Wen-Xin Fan, Dong-Hang Tan, Ji-Lin Li, Wen-Xin Lv
Publikováno v:
Angewandte Chemie. 130:16782-16786
Organofluorine compounds are widely used in pharmaceutical, agrochemical, and materials sciences. The syntheses and applications of fluorinated organoborons facilitate the rapid and modular assemblies of fluorine-containing molecules because of the v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a30e6ce33e8a1642370bf8ccae8b9d6
https://doi.org/10.1002/ange.201810204
https://doi.org/10.1002/ange.201810204
Autor:
Wei-Wei Ji, Hui Gao, Qingjiang Li, Dong-Hang Tan, Yao-Fu Zeng, Honggen Wang, E Lin, Wen-Xin Fan
Publikováno v:
Advanced Synthesis & Catalysis. 360:1032-1037
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2381972ef6bd1795e42db3475e0a4eda
https://doi.org/10.1002/adsc.201701497
https://doi.org/10.1002/adsc.201701497
Publikováno v:
Chemical Communications. 54:5907-5910
A novel synthesis of α-CF3 and α-CF2H amines via the aminofluorination of gem-difluoroalkenes and mono-fluoroalkenes, respectively, is reported. The method employs Selectfluor as an electrophilic fluorine source and acetonitrile as a nitrogen sourc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd2cae79428a09343c6f527a239ccabc
https://doi.org/10.1039/c8cc03364a
https://doi.org/10.1039/c8cc03364a
Publikováno v:
Chemical communications (Cambridge, England). 54(46)
A novel synthesis of α-CF3 and α-CF2H amines via the aminofluorination of gem-difluoroalkenes and mono-fluoroalkenes, respectively, is reported. The method employs Selectfluor as an electrophilic fluorine source and acetonitrile as a nitrogen sourc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6376815b1ca28ab05e3a4bd48b7464bb
https://pubmed.ncbi.nlm.nih.gov/29789842
https://pubmed.ncbi.nlm.nih.gov/29789842