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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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
Publication:	TETRAHEDRON
Publisher:	PERGAMON-ELSEVIER SCIENCE LTD
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
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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