Pd-catalyzed enantioselective intramolecular Heck reaction to access disubstituted dihydroisoquinolinone with a terminal olefin
A first palladium-catalyzed asymmetric intramolecular Heck reaction for the construction 3,4-dihydro-1-(2H)-isoquinolinone containing the quaternary carbon chiral center has been developed. The salient features of this reaction include high efficiency, high enantioselectivity, the novel chiral ligan...
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KeAi Communications Co. Ltd.
2021
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oai:doaj.org-article:dd732803d4564fb7916cd1148cefcfa42021-12-02T05:03:58ZPd-catalyzed enantioselective intramolecular Heck reaction to access disubstituted dihydroisoquinolinone with a terminal olefin2666-554910.1016/j.gresc.2021.10.006https://doaj.org/article/dd732803d4564fb7916cd1148cefcfa42021-11-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2666554921000879https://doaj.org/toc/2666-5549A first palladium-catalyzed asymmetric intramolecular Heck reaction for the construction 3,4-dihydro-1-(2H)-isoquinolinone containing the quaternary carbon chiral center has been developed. The salient features of this reaction include high efficiency, high enantioselectivity, the novel chiral ligand and diverse transformations.Sanliang LiQiaoyu ChenZhan-Ming ZhangJunliang ZhangKeAi Communications Co. Ltd.articlePalladiumAlkenesAsymmetric catalysisQuaternary stereocenterDihydroisoquinolinoneChemical technologyTP1-1185BiochemistryQD415-436ENGreen Synthesis and Catalysis, Vol 2, Iss 4, Pp 374-376 (2021) |
institution |
DOAJ |
collection |
DOAJ |
language |
EN |
topic |
Palladium Alkenes Asymmetric catalysis Quaternary stereocenter Dihydroisoquinolinone Chemical technology TP1-1185 Biochemistry QD415-436 |
spellingShingle |
Palladium Alkenes Asymmetric catalysis Quaternary stereocenter Dihydroisoquinolinone Chemical technology TP1-1185 Biochemistry QD415-436 Sanliang Li Qiaoyu Chen Zhan-Ming Zhang Junliang Zhang Pd-catalyzed enantioselective intramolecular Heck reaction to access disubstituted dihydroisoquinolinone with a terminal olefin |
description |
A first palladium-catalyzed asymmetric intramolecular Heck reaction for the construction 3,4-dihydro-1-(2H)-isoquinolinone containing the quaternary carbon chiral center has been developed. The salient features of this reaction include high efficiency, high enantioselectivity, the novel chiral ligand and diverse transformations. |
format |
article |
author |
Sanliang Li Qiaoyu Chen Zhan-Ming Zhang Junliang Zhang |
author_facet |
Sanliang Li Qiaoyu Chen Zhan-Ming Zhang Junliang Zhang |
author_sort |
Sanliang Li |
title |
Pd-catalyzed enantioselective intramolecular Heck reaction to access disubstituted dihydroisoquinolinone with a terminal olefin |
title_short |
Pd-catalyzed enantioselective intramolecular Heck reaction to access disubstituted dihydroisoquinolinone with a terminal olefin |
title_full |
Pd-catalyzed enantioselective intramolecular Heck reaction to access disubstituted dihydroisoquinolinone with a terminal olefin |
title_fullStr |
Pd-catalyzed enantioselective intramolecular Heck reaction to access disubstituted dihydroisoquinolinone with a terminal olefin |
title_full_unstemmed |
Pd-catalyzed enantioselective intramolecular Heck reaction to access disubstituted dihydroisoquinolinone with a terminal olefin |
title_sort |
pd-catalyzed enantioselective intramolecular heck reaction to access disubstituted dihydroisoquinolinone with a terminal olefin |
publisher |
KeAi Communications Co. Ltd. |
publishDate |
2021 |
url |
https://doaj.org/article/dd732803d4564fb7916cd1148cefcfa4 |
work_keys_str_mv |
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_version_ |
1718400681908371456 |