Enantioselective total synthesis of polyoxygenated cyclohexanoids: (+)-streptol, ent-RKTS-33 and putative '(+)-parasitenone'. identity of parasitenone with (+)-epoxydon

Mehta, Goverdhan ; Pujar, Shashikant R. ; Ramesh, Senaiar S. ; Islam, Kabirul (2005) Enantioselective total synthesis of polyoxygenated cyclohexanoids: (+)-streptol, ent-RKTS-33 and putative '(+)-parasitenone'. identity of parasitenone with (+)-epoxydon Tetrahedron Letters, 46 (19). pp. 3373-3376. ISSN 0040-4039

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Official URL: http://linkinghub.elsevier.com/retrieve/pii/S00404...

Related URL: http://dx.doi.org/10.1016/j.tetlet.2005.03.087

Abstract

Short, simple and enantioselective syntheses of the natural product (+)-streptol, the non-peptide apoptosis inhibitor ent-RKTS-33 and the putative structure of 'parasitenone' have been accomplished from the readily available chiral building block. 'Parasitenone' has been shown to be identical with the known natural product epoxydon.

Item Type:	Article
Source:	Copyright of this article belongs to Elsevier Science.
ID Code:	28943
Deposited On:	18 Dec 2010 05:46
Last Modified:	17 May 2016 11:56

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