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Enantioselective synthesis of macrolactone core of the natural product Sch725674

Sunnam, Sunil Kumar and Prasad, Kavirayani R (2014) Enantioselective synthesis of macrolactone core of the natural product Sch725674. In: TETRAHEDRON, 70 (12). pp. 2096-2101.

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Official URL: http://dx.doi.org/10.1016/j.tet.2014.02.008

Abstract

An enantioselective synthesis of the macrolactone core of natural product Sch725674 was accomplished from furfural. Key reactions in assembly of the macrolactone are the use of furan as a but-2-ene-dione equivalent and ring closing metathesis. (C) 2014 Elsevier Ltd. All rights reserved.

Item Type: Journal Article
Additional Information: copyright for this article belongs to PERGAMON-ELSEVIER SCIENCE LTD, ENGLAND
Keywords: Macrolide; Total synthesis; Natural products; Sch725674
Department/Centre: Division of Chemical Sciences > Organic Chemistry
Depositing User: Id for Latest eprints
Date Deposited: 24 Apr 2014 07:35
Last Modified: 24 Apr 2014 07:35
URI: http://eprints.iisc.ac.in/id/eprint/48906

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