Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Shi‐Jiang He"'
Autor:
Sheng‐Qi Qiu, Yu Chen, Xiang‐Jun Peng, Shi‐Jiang He, Jun Kee Cheng, Yong‐Bin Wang, Shao‐Hua Xiang, Jun Song, Peiyuan Yu, Junmin Zhang, Bin Tan
Publikováno v:
Angewandte Chemie International Edition. 61
The application of Suzuki-Miyaura coupling reaction to forge the atropisomeric biaryls has seen remarkable progress but exploration of this chemistry to directly forge chiral C(aryl)-C(alkene) axis is underdeveloped. The replacement of arene substrat
Publikováno v:
Angewandte Chemie (International ed. in English). 62(1)
Anthrones and analogues are structural cores shared by diverse pharmacologically active natural and synthetic compounds. The sp
Publikováno v:
Chemical Science
We report a three-component olefin reductive dicarbofunctionalization for constructing alkylborates, specifically, nickel-catalyzed reductive dialkylation and alkylarylation of vinyl boronates with a variety of alkyl bromides and aryl iodides. This r
Publikováno v:
Journal of the American Chemical Society. 142:214-221
Substantial advances in enantioconvergent C(sp3)-C(sp3) bond formation reactions have been made in recent years through the use of transition-metal-catalyzed cross-coupling reactions of racemic secondary alkyl electrophiles with organometallic reagen
Publikováno v:
Chemical Science
Synthesis of functionalized gem-difluoroalkenes was achieved through nickel-catalyzed allylic defluorinative alkylation of trifluoromethyl alkenes with reductive decarboxylation of redox-active esters.
Herein, we report a nickel-catalyzed allyli
Herein, we report a nickel-catalyzed allyli
We report a three-component olefin reductive dicarbofunctionalization for constructing densely functionalized alkylborates, specifically, nickel-catalyzed reductive dialkylation and alkylarylation of vinyl boronates with a variety of alkyl bromides a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::26d9f82d32eb914b772db15dd4db6c72
https://doi.org/10.26434/chemrxiv.11821341
https://doi.org/10.26434/chemrxiv.11821341
Autor:
Yao Fu, Xiao-Xu Wang, Bing Wang, Bin Xiao, Yan Wang, Xi Lu, Yinuo Yang, Tian-Jun Gong, Shi-Jiang He
Publikováno v:
Organic letters. 20(17)
A copper-catalyzed borylation/benzylic cyanation of vinylarenes whose regioselectivity is seemly common but scarcely achieved is reported. This unprecedented regioselectivity is realized through a structure-distinctive cyanating reagent, dimethylmalo