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Synthesis of Phenylpropanoids via Matsuda-Heck Coupling of Arene Diazonium Salts

  • The Pd-catalyzed Heck-type coupling (Matsuda Heck reaction) of electron rich arene diazonium salts with electron deficient olefins has been exploited for the synthesis of phenylpropanoid natural products. Examples described herein are the naturally occurring benzofurans methyl wutaifuranate, wutaifuranol, wutaifuranal, their 7-methoxy derivatives, and the O-prenylated natural products boropinols A and C.

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Author details:Bernd SchmidtORCiDGND, Felix Wolf
DOI:https://doi.org/10.1021/acs.joc.7b00447
ISSN:0022-3263
Pubmed ID:https://pubmed.ncbi.nlm.nih.gov/28394127
Title of parent work (English):The journal of organic chemistry
Publisher:American Chemical Society
Place of publishing:Washington
Publication type:Article
Language:English
Year of first publication:2017
Publication year:2017
Release date:2020/04/20
Volume:82
Number of pages:10
First page:4386
Last Page:4395
Organizational units:Mathematisch-Naturwissenschaftliche Fakultät / Institut für Chemie
Peer review:Referiert
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