Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Huai‐Ri Sun"'
Autor:
Hui Yang, Huai-Ri Sun, Rui-Qing He, Le Yu, Wei Hu, Jie Chen, Sen Yang, Gong-Gu Zhang, Ling Zhou
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-9 (2022)
There is great interest in methods for catalytic enantioselective construction of axially chiral compounds found in natural products. Here, the authors develop a cycloaddition strategy for atroposelective construction of indole-based biaryls via chir
Externí odkaz:
https://doaj.org/article/d88d8d0394084bf69a7c62c10c1a5696
Autor:
Qing-Song Jian, Bo-Bo Gou, Shao-Jie Wang, Huai-Ri Sun, Atif Sharif, Yong-Qiang Wang, Ling Zhou, Jie Chen
Publikováno v:
Organic Chemistry Frontiers. 10:1936-1941
A simple and efficient heteroannulation reaction for the synthesis of 1-(quinolin-2-yl)naphthalen-2-ols has been developed, and the products can be transformed to axially chiral arylquinolines by dynamic kinetic resolution.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8dcdcc4574e220009bb7ab49871b7838
https://doi.org/10.1039/d2qo01813f
https://doi.org/10.1039/d2qo01813f
Publikováno v:
Chemistry – A European Journal. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::22ab6d4174457c8174612fa32ea32f98
https://doi.org/10.1002/chem.202382761
https://doi.org/10.1002/chem.202382761
Publikováno v:
Chemistry – A European Journal. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb50b6dd6ee4822546628f09c8a776c9
https://doi.org/10.1002/chem.202300183
https://doi.org/10.1002/chem.202300183
Publikováno v:
Organic Letters. 24:4316-4321
An efficient dehydrogenative inverse electron demand Diels-Alder reaction of isopropyl and prenyl benzene derivatives with electron-deficient dienes followed by decarboxylation has been reported for the first time. The much broader substrate scope of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6b5b79556519daa6df24902cbcac696
https://doi.org/10.1021/acs.orglett.2c01197
https://doi.org/10.1021/acs.orglett.2c01197
Publikováno v:
The Journal of Organic Chemistry. 86:17673-17683
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c81b06d060e964a3333e7b4f255e9e51
https://doi.org/10.1021/acs.joc.1c01912
https://doi.org/10.1021/acs.joc.1c01912
Publikováno v:
Angewandte Chemie International Edition. 61
Here we report a new type of chiral all-carbon tetrasubstituted VQMs generated via chiral phosphoric acids catalyzed nucleophilic addition of 2-alkynylnaphthols to o-quinone methides or imines, which can be captured intramolecularly as a result of cy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bfdcf12340f0fdd9017d4a4b29c5e26
https://doi.org/10.1002/anie.202208174
https://doi.org/10.1002/anie.202208174
Publikováno v:
Organic Letters. 21:9829-9835
Stereoselective [1 + 1 + 4 + 4] dimerization of 1-styrylnaphthols has been developed by using Selectfluor as the oxidant for the first time. The reaction was compatible with various functional groups, giving a class of ethanodinaphtho[b,f][1,5]dioxoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2225f217a0a970456a401aa99b1e6649
https://doi.org/10.1021/acs.orglett.9b03587
https://doi.org/10.1021/acs.orglett.9b03587
Publikováno v:
Organic Letters. 21:80-84
Phenanthrene is an important structural motif in chemistry and materials science, and many synthetic routes have been developed to construct its skeleton. However, synthesis of unsymmetric phenanthrenes remains a challenge. Here, an efficient one-pot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::afd9a47edd76b682c01b5521257cfebd
https://doi.org/10.1021/acs.orglett.8b03511
https://doi.org/10.1021/acs.orglett.8b03511
Publikováno v:
Organic letters. 21(17)
Asymmetric Prins cyclization of in situ generated quinone methides and o-aminobenzaldehyde has been developed with chiral phosphoric acid as an efficient catalyst. This unconventional method provides a facile access to diverse functionalized trans-fu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3684eff2bd0c423d23044f3e1256c0e
https://pubmed.ncbi.nlm.nih.gov/31414820
https://pubmed.ncbi.nlm.nih.gov/31414820