Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Tianxin Hao"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 17, Iss 1, Pp 2462-2476 (2021)
Great progress has been made in the tandem annulation of enynes in the past few years. This review only presents the corresponding reactions of 1,3-enyne structural motifs to provide the functionalized pyridine and pyrrole derivatives. The functional
Externí odkaz:
https://doaj.org/article/1e07410fdf0549298a2abc5f9a635c03
Autor:
Yi Liu, Wei Gao, Sitian Yuan, Mengjia Ni, Tianxin Hao, Cuiying Zeng, Xinyi Xu, Yang Fu, Yiyuan Peng, Qiuping Ding
Publikováno v:
Organic & Biomolecular Chemistry. 21:4257-4263
AgI-catalyzed one-pot sulfenylation/cyclization of o-isocyanodiaryl amines has been described for the preparation of 11-sulfenyl dibenzodiazepines in moderate to good yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::afa7f78d27d6f5ae5e519abcb64744dd
https://doi.org/10.1039/d3ob00220a
https://doi.org/10.1039/d3ob00220a
Publikováno v:
Chemical Communications. 58:10985-10988
A radical addition/cyclization reaction of o-isocyanodiaryl amines has been developed for the efficient synthesis of potentially bioactive dibenzo[b,e][1,4]diazepine-11-carboxylates and dibenzo[b,e][1,4]diazepine-11-carboxamides.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::987b9eaa1468ad3532ec6c2dbf9ffe55
https://doi.org/10.1039/d2cc04348c
https://doi.org/10.1039/d2cc04348c
Publikováno v:
Chemical communications (Cambridge, England). 58(78)
A radical addition/cyclization reaction of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f3add7163dd612b0d94aa32bdca0fc3a
https://pubmed.ncbi.nlm.nih.gov/36093760
https://pubmed.ncbi.nlm.nih.gov/36093760
Publikováno v:
Tetrahedron. 79:131832
A copper-mediated formal [5 + 1] oxidative annulation of 2-vinylanilines and glyoxylic acid to 4-arylated quinolines was developed. A series of 4-arylated quinoline derivatives were obtained in good to excellent yields. This protocol could be carried
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2b81d7d5aa5582b7d1209716a47299f
https://doi.org/10.1016/j.tet.2020.131832
https://doi.org/10.1016/j.tet.2020.131832