Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Xuezhen Kou"'
Publikováno v:
Pharmaceutical Fronts, Vol 06, Iss 03, Pp e237-e251 (2024)
Externí odkaz:
https://doaj.org/article/1893cbd60aba4af19abc960545dfcb59
Publikováno v:
Advanced Science, Vol 11, Iss 23, Pp n/a-n/a (2024)
Abstract Asymmetric sequential hydrogenations of α‐methylene γ‐ or δ‐keto carboxylic acids are established in one‐pot using a bimetallic Ru/Ru catalyst system, achieving the stereodivergent synthesis of all four stereoisomers of both chira
Externí odkaz:
https://doaj.org/article/8394011886f0430984045730453eb20b
Autor:
Kevin G. M. Kou, Xuezhen Kou
Publikováno v:
ACS Catalysis. 10:3103-3109
Carbon–hydrogen (C–H) bond functionalization streamlines synthesis by increasing step- and atom-economies. This approach, catalyzed by Rh(III), is combined with the α-arylation of ketone-derived si...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68df53ac76625e51a7430c1f9e8aca08
https://doi.org/10.1021/acscatal.9b05622
https://doi.org/10.1021/acscatal.9b05622
Publikováno v:
Tetrahedron Letters. 60:1148-1152
A PhI(OAc)2-promoted dioxygenation of allyl oximes, including one alkoxylation, has been developed. This reaction can give isoxazoline products bearing two contiguous tetrasubstituted carbons. Various oximes substrates bearing different aryl groups a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::25297d343405bddf88e3d576af3953de
https://doi.org/10.1016/j.tetlet.2019.03.046
https://doi.org/10.1016/j.tetlet.2019.03.046
Publikováno v:
Chinese Journal of Organic Chemistry. 42:1747
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e5383edd4fc8f5aa7366f9afaa58d81
https://doi.org/10.6023/cjoc202112040
https://doi.org/10.6023/cjoc202112040
Publikováno v:
Chemistry - An Asian Journal. 13:1897-1901
A PdII -catalyzed oxidative tandem cyclization was developed for the construction of fused 5,6-bicyclic N, O-heterocycles. This reaction was enabled by the combined use of a 3-methylpyridine ligand and pentafluorobenzoic acid additive. A range of het
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a081f54e85eb4dfdd9f2438175563d2d
https://doi.org/10.1002/asia.201800646
https://doi.org/10.1002/asia.201800646
Autor:
Xuezhen Kou, Kevin G. M. Kou
Publikováno v:
ACS Catalysis. 11:11510-11510
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1669d0f4e19430e1a0275061557fc721
https://doi.org/10.1021/acscatal.1c03643
https://doi.org/10.1021/acscatal.1c03643
Publikováno v:
Tetrahedron Letters. 58:285-288
A Pd(II)-catalyzed cyclization using oxidative olefin diamination was developed for the preparation of isoindolinones from ortho-olefinic N-methoxybenzamides. Using the optimized reaction conditions, the desired products were obtained in up to 90% yi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::60cc2f96266af377684d94b51db9820e
https://doi.org/10.1016/j.tetlet.2016.11.113
https://doi.org/10.1016/j.tetlet.2016.11.113
Publikováno v:
Journal of the American Chemical Society. 140(24)
We have developed an asymmetric aza-Wacker-type cyclization of N-Ts hydrazine-tethered tetrasubstituted olefins, affording optically active pyrazolines bearing chiral tetrasubstituted carbon stereocenters. This reaction is tolerant to a broad range o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6ce1c01bd69f7b0c55691eb5506bb34
https://pubmed.ncbi.nlm.nih.gov/29804449
https://pubmed.ncbi.nlm.nih.gov/29804449
Autor:
Chenghao, Ye, Xuezhen, Kou, Jingzhao, Xia, Guoqiang, Yang, Li, Kong, Quhao, Wei, Wanbin, Zhang
Publikováno v:
Chemistry, an Asian journal.
A Pd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fb3f0153c1776922b87264d69cbe2165
https://pubmed.ncbi.nlm.nih.gov/29851272
https://pubmed.ncbi.nlm.nih.gov/29851272