Enantiospecific formal total synthesis of (+)-dihydrokawain-5-ol

Metri, PK (2020) Enantiospecific formal total synthesis of (+)-dihydrokawain-5-ol. In: Synthetic Communications, 50 (9). pp. 1361-1366.

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Abstract

Formal total synthesis of dihydrokawain-5-ol is accomplished starting from tartaric acid. Key reactions include Horner�Wadsworth�Emmons olefination, sodium borohydride mediated stereoselective reduction, orthogonal protection and deprotection of alcohols and ring closing metathesis. © 2020, © 2020 Taylor & Francis Group, LLC.

Item Type:	Journal Article
Publication:	Synthetic Communications
Publisher:	Taylor and Francis Inc.
Additional Information:	Copyright for this article belongs to Taylor and Francis
Keywords:	Biological activities, metathesis, natural products, total synthesis
Department/Centre:	Division of Chemical Sciences > Organic Chemistry
Date Deposited:	02 Sep 2020 08:56
Last Modified:	02 Sep 2020 08:57
URI:	http://eprints.iisc.ac.in/id/eprint/64985

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