Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Hetao Xu"'
Autor:
Qiuling Song, Shihui Wang, Wangyang Li, Jian Qiu, Mengyuan Hou, Kai Yang, Qianqian Shi, Hetao Xu, Shuai Wang, Guan Zhang, Yu Lan, Chaokun Li, Cece Wang, Lu Zhou, Shi-Jun Li
Publikováno v:
CCS Chemistry. 4:1671-1679
Contrary to the traditional implementation as a difluoromethyl group and recently disclosed role of C1 synthons in synthetic organic chemistry, difluorocarbene (:CF2) is reported herein to proceed ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4bbc3e30fa552370d78f273b56b26643
https://doi.org/10.31635/ccschem.021.202100979
https://doi.org/10.31635/ccschem.021.202100979
Publikováno v:
Organic Letters. 23:7776-7780
Herein we present a transition-metal-free cross-coupling reaction of isatogens with boronic acids through a 1,4-metalate shift of a boron "ate" complex. This coupling reaction provides a feasible method to deliver valuable 2,2-disubstituted indolin-3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2953fa1b819b579552e0aa3d41155580
https://doi.org/10.1021/acs.orglett.1c02808
https://doi.org/10.1021/acs.orglett.1c02808
Publikováno v:
Organic Letters. 22:7874-7878
An important framework of o-amino benzofuranthioethers was constructed by Cu-catalyzed arylative cyclization of N-tosylhydrazone-bearing thiocarbamates with silylaryl triflates or ArI. This transformation provides a novel strategy for the synthesis o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f8256e0e361c28fcbcb26c523345362
https://doi.org/10.1021/acs.orglett.0c02778
https://doi.org/10.1021/acs.orglett.0c02778
Autor:
Feng Zhang, Guan Zhang, Chenglan Wang, Yixian Lou, Liang-Wen Qi, Peiyuan Yu, Kai Yang, Wangyang Li, Tongchang Fang, Lu Zhou, Hetao Xu, Qiuling Song
Publikováno v:
Angewandte Chemie International Edition. 59:3294-3299
A new chiral Brønsted acid, generated in situ from a chiral phosphoric acid boron (CPAB) complex and water, was successfully applied to asymmetric indole reduction. This "designer acid catalyst", which is more acidic than TsOH as suggested by DFT ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d54dc5a4026404155a5877dcab8ce3c
https://doi.org/10.1002/anie.201913656
https://doi.org/10.1002/anie.201913656
Publikováno v:
Organic letters. 22(20)
An important framework of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::aced1353c52250b3baa9f64ab403b6e8
https://pubmed.ncbi.nlm.nih.gov/32990445
https://pubmed.ncbi.nlm.nih.gov/32990445