Total synthesis of the macrolactone AKML-B

Kesavulu, G and Silambarasan, K and Prasad, KR (2024) Total synthesis of the macrolactone AKML-B. In: Tetrahedron, 166 .

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Abstract

Total synthesis of the 24-memebred macrolactone AKML-B was accomplished starting from a chiral furyl carbinol. The key reaction in the present approach includes the oxidation of furan to an unsaturated keto aldehyde and the use of Ring Closing Metathesis (RCM) reaction for the macrolactone formation. © 2024 Elsevier Ltd

Item Type:	Journal Article
Publication:	Tetrahedron
Publisher:	Elsevier Ltd
Additional Information:	The copyright for this article belongs to the Publisher.
Department/Centre:	Division of Chemical Sciences > Organic Chemistry
Date Deposited:	17 Sep 2024 11:03
Last Modified:	17 Sep 2024 11:03
URI:	http://eprints.iisc.ac.in/id/eprint/86111

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