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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Autores principales: Sanliang Li, Qiaoyu Chen, Zhan-Ming Zhang, Junliang Zhang
Formato: article
Lenguaje:EN
Publicado: KeAi Communications Co. Ltd. 2021
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Acceso en línea:https://doaj.org/article/dd732803d4564fb7916cd1148cefcfa4
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spelling 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 AT sanliangli pdcatalyzedenantioselectiveintramolecularheckreactiontoaccessdisubstituteddihydroisoquinolinonewithaterminalolefin
AT qiaoyuchen pdcatalyzedenantioselectiveintramolecularheckreactiontoaccessdisubstituteddihydroisoquinolinonewithaterminalolefin
AT zhanmingzhang pdcatalyzedenantioselectiveintramolecularheckreactiontoaccessdisubstituteddihydroisoquinolinonewithaterminalolefin
AT junliangzhang pdcatalyzedenantioselectiveintramolecularheckreactiontoaccessdisubstituteddihydroisoquinolinonewithaterminalolefin
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