Synthesis of various 2H-benzopyran compounds and their kinetic resolution by asymmetric hydrolysis of their racemic acetates mediated by lipases

dc.contributor.authorJ. Y. Goujon
dc.contributor.authorF. Zammattio
dc.contributor.authorB. Kirschleger
dc.date.accessioned2012-11-09T09:06:56Z
dc.date.accessioned2025-02-17T13:59:35Z
dc.date.available2012-11-09T09:06:56Z
dc.date.issued2012-11-09
dc.descriptionThe preparation of 2H-benzopyrans from bromophenols and tertiary allylic alcohols is described. The reaction is characterised by its mildness, good yields and ease of work-up. Kinetic resolution of the latter up to 95% ee was obtained by using enzyme-catalysed enantioselective hydrolysis. # 2000 Elsevier Science Ltd. All rights reserved.en_US
dc.description.abstractThe preparation of 2H-benzopyrans from bromophenols and tertiary allylic alcohols is described. The reaction is characterised by its mildness, good yields and ease of work-up. Kinetic resolution of the latter up to 95% ee was obtained by using enzyme-catalysed enantioselective hydrolysis. # 2000 Elsevier Science Ltd. All rights reserved.en_US
dc.identifier.urihttps://dl.ftveti.edu.et/handle/123456789/3978
dc.language.isoenen_US
dc.subjectSynthesis of various 2H-benzopyran compounds and their kinetic resolution by asymmetric hydrolysis of their racemic acetates mediated by lipasesen_US
dc.titleSynthesis of various 2H-benzopyran compounds and their kinetic resolution by asymmetric hydrolysis of their racemic acetates mediated by lipasesen_US
dc.typeArticleen_US

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