Total Synthesis of 4-Ketoclonostachydiol

Yadav, Jhillu ; Vardhan, Vijaya ; Das, Saibal (2014) Total Synthesis of 4-Ketoclonostachydiol Synthesis, 46 (17). pp. 2347-2352. ISSN 0039-7881

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Official URL: http://doi.org/10.1055/S-0033-1339121

Related URL: http://dx.doi.org/10.1055/S-0033-1339121

Abstract

A facile total synthesis of nonsymmetrical 14-membered macrocyclic bis-lactone, 4-ketoclonostachydiol has been demonstrated in a convergent approach. The synthetic strategy has been unambiguously successful towards incorporating all the three stereogenic centers present in the molecule with an overall yield of 0.9%. The key synthetic step includes MacMillan hydroxylation and Grubbs ring-closing metathesis reactions to furnish the core skeleton.

Item Type:Article
Source:Copyright of this article belongs to Georg Thieme Verlag KG.
ID Code:135663
Deposited On:17 Jul 2023 08:02
Last Modified:17 Jul 2023 08:02

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