Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Zhenxiu He"'
Autor:
Chunxiang Pan, Yunyan Meng, Yao Deng, Bingjie Zhou, Jingchao Chen, Zhenxiu He, Weiqing Sun, Ruhima Khan, Baomin Fan
Publikováno v:
Chinese Journal of Chemistry. 40:2040-2046
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b582c7f31aebb8895ee432932a8f53d1
https://doi.org/10.1002/cjoc.202200144
https://doi.org/10.1002/cjoc.202200144
Publikováno v:
Asian Journal of Organic Chemistry. 11
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b393389c3dd9b6f4a1dd1c0e6f0d1fe2
https://doi.org/10.1002/ajoc.202200336
https://doi.org/10.1002/ajoc.202200336
Autor:
Lin Wang, Haojie Liu, Zhenxiu He, Jingchao Chen, Guoli Shen, Yang Luo, Zhimin Su, Baomin Fan, Yongyun Zhou
Publikováno v:
Organic & Biomolecular Chemistry. 19:3601-3610
The zinc salt-catalyzed reduction of α-aryl imino esters, diketones and phenylacetylenes with water as hydrogen source and zinc as reductant was successfully conducted. The presented method provides a low-cost, environmentally friendly and practical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8240f86b98f86c26a6f17c21454198f6
https://doi.org/10.1039/d1ob00155h
https://doi.org/10.1039/d1ob00155h
Publikováno v:
Advanced Synthesis & Catalysis. 361:4495-4499
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::daacd66dbc57f4e64f109794a87cbcea
https://doi.org/10.1002/adsc.201900622
https://doi.org/10.1002/adsc.201900622
Autor:
Li Sida, Baomin Fan, Gaowei Wang, Sun Weiqing, Jingchao Chen, Jianxiao Ni, Yongyun Zhou, Zhenxiu He
Publikováno v:
Advanced Synthesis & Catalysis. 361:3543-3547
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b90dd514d1594d42e2b449370d58ae51
https://doi.org/10.1002/adsc.201900380
https://doi.org/10.1002/adsc.201900380
Publikováno v:
Organic & Biomolecular Chemistry. 17:10142-10147
Rhodium-catalyzed transfer hydrogenation of quinoxalines with water as a hydrogen source was reported. The reaction allowed the simple preparation of tetrahydroquinoxalines under mild conditions. The deuterium-labelling experiment confirmed that wate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5774fedbfde3cb9caabc53aad3e8c07c
https://doi.org/10.1039/c9ob02095k
https://doi.org/10.1039/c9ob02095k
Publikováno v:
Chemistry - An Asian Journal. 13:2431-2434
Enantioselective [2+2] cycloaddition reaction of azabenzonorbornadienes and oxabenzonorbornadienes with internal alkynes has been enabled by a catalyst system comprising Ni(COD)2 and (R)-SIPHOS-Ph-Mor. This transformation represents the first asymmet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42b030ce99d605436cd3b59e5cd04459
https://doi.org/10.1002/asia.201800492
https://doi.org/10.1002/asia.201800492
Publikováno v:
Organic Letters. 20:1291-1294
A mild, efficient, and novel rhodium catalyzed asymmetric cyclization–addition domino reaction of oxa/azabenzonorbornadienes and 1,6-enynes is documented. Through the use of a [Rh(COD)2]BF4-(R)-An-SDP catalytic system, highly enantioenriched cycliz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c8d168d579ff8cf6f327c0a9073d74b
https://doi.org/10.1021/acs.orglett.7b04044
https://doi.org/10.1021/acs.orglett.7b04044
Publikováno v:
Organic Chemistry Frontiers. 5:1108-1112
A general strategy for the asymmetric allylation and benzylation of heterobicyclic alkenes is described by employing in situ generated organozinc halides. This methodology features the application of a co-catalytic system comprising chiral cobalt com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09eaa3d55bc00858d3277faa897d0195
https://doi.org/10.1039/c7qo01064h
https://doi.org/10.1039/c7qo01064h
Publikováno v:
Advanced Synthesis & Catalysis. 360:427-431
The asymmetric [2+2] cycloaddition reactions of alkenes with alkynes are interesting as it has provided a powerful method for the construction of fused and strained cyclobutenes with multiple chiral centers. In this paper, we report the establishment
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c75a36c54303d250e6562329925a93c0
https://doi.org/10.1002/adsc.201701133
https://doi.org/10.1002/adsc.201701133