Zobrazeno 1 - 10
of 144
pro vyhledávání: '"Rongxiu Zhu"'
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-10 (2022)
Catalytic kinetic resolution of racemates is among the best ways to prepare enantiopure compounds, but this process is difficult with organic azides given the small size of the azido group. Here, the authors show kinetic resolution of cyclic benzylic
Externí odkaz:
https://doaj.org/article/ac9caa54932c4afda44abdc87edcd24e
Publikováno v:
University Chemistry. 2023, Vol. 38 Issue 2, p271-276. 6p.
Publikováno v:
Journal of Catalysis. 418:263-272
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16709a9fdfcd5cc358896497a5dda33c
https://doi.org/10.1016/j.jcat.2023.01.014
https://doi.org/10.1016/j.jcat.2023.01.014
Publikováno v:
Chemical Science. 14:4580-4588
DFT calculations shows an unexpected mechanism in the photoredox/copper-catalyzed carbocyanation of 1,3-diene, which involves CuI-only catalysis and the single electron transfer from the allyl radical to the oxidized photocatalyst.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e57c69dc016c398b8cecf69b33f575d
https://doi.org/10.1039/d3sc00002h
https://doi.org/10.1039/d3sc00002h
Publikováno v:
ACS Catalysis. 12:2290-2301
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8195d6070c09d6887572c6ffd0e4f459
https://doi.org/10.1021/acscatal.1c05025
https://doi.org/10.1021/acscatal.1c05025
Publikováno v:
Organic Chemistry Frontiers. 9:147-155
In a new mechanism for photosensitizer-free visible-light-mediated gold-catalyzed cross-coupling, the π–π complex between aryldiazonium salts and arylboronic acids acts as a photoinitiator.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::449d23eba3dd009e46604157ab4b39df
https://doi.org/10.1039/d1qo01464a
https://doi.org/10.1039/d1qo01464a
Autor:
Xiaobin Li, Rongxiu Zhu, Fei Xie, Rui-Juan Li, Xiao-Yi Luan, Qiaobian He, Ke Xu, Yanan Qiao, Yuliang Xu, Hong-Xiang Lou
Publikováno v:
Organic Letters. 23:7751-7754
Two pairs of diastereoisomeric isoindoline alkaloids, xylarins A-D (1-4), were isolated from the endolichenic fungus Xylaria sp. Xylarins A and B (1 and 2) possess a previously undescribed 5/6/5-5/6 polycyclic scaffold, featuring a combination of a n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9a6dad9e51209d81592e8a3b22bb8b26
https://doi.org/10.1021/acs.orglett.1c02730
https://doi.org/10.1021/acs.orglett.1c02730
Publikováno v:
Journal of Molecular Modeling. 28
Most hydrazone compounds prefer the azine tautomeric states. However, oxygen-/sulfur-substituted compounds prefer hydrazone tautomers. In this study, density functional theory at M062X level with the basis set of 6-311 + + g(2d, 2p), with MP2/cc-pVTZ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6a88a8229a2cb63683deb0f0a574c5a
https://doi.org/10.1007/s00894-022-05387-2
https://doi.org/10.1007/s00894-022-05387-2
Publikováno v:
Angewandte Chemie. 133:18647-18651
The asymmetric construction of vicinal quaternary carbon stereocenters with at least one moiety in acyclic systems is a formidable challenge. We disclose a solution involving diastereo- and enantioselective oxidative 1,6-conjugate addition. The pract
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f30fab1e57a82e97aa7326ac58b5faa
https://doi.org/10.1002/ange.202105594
https://doi.org/10.1002/ange.202105594
Autor:
Ai-Hong Su, Jing-Jing Han, Jiao-Zhen Zhang, Xu-Yuan Liu, Hong-Xiang Lou, Ze-Jun Xu, Yuliang Xu, Yan Zong, Rongxiu Zhu, Ming-Zhu Zhu
Publikováno v:
Angewandte Chemie International Edition. 60:15286-15290
An enantioselective synthetic approach for preparing manginoids and guignardones, two types of biogenetically related meroterpenoids, is reported. This bioinspired and divergent synthesis employs an oxidative 1,3-dicarbonyl radical-initiated cyclizat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2e833f0de89769dbc042c770e59e485
https://doi.org/10.1002/anie.202104182
https://doi.org/10.1002/anie.202104182