A new approach to A/B ring analogue of eleutherobin and sarcodictyns through a sequence of highly diastereofaceselective Diels-Alder reaction and ring opening-ring closing metathesis (RO-RCM)

Malik, Chanchal K. ; Hossain, Firoj ; Ghosh, Subrata (2009) A new approach to A/B ring analogue of eleutherobin and sarcodictyns through a sequence of highly diastereofaceselective Diels-Alder reaction and ring opening-ring closing metathesis (RO-RCM) Tetrahedron Letters, 50 (25). pp. 3063-3066. ISSN 0040-4039

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Official URL: http://www.sciencedirect.com/science/article/pii/S...

Related URL: http://dx.doi.org/10.1016/j.tetlet.2009.04.033

Abstract

An approach to the construction of A/B ring analogue of antitumour compounds eleutherobin and sarcodictyns is described. The key steps involve a highly diastereofaceselective Diels-Alder reaction of a dienophile containing a furanosugar moiety with cyclopentadiene and ring opening-ring closing metathesis of the resulting adduct.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
Keywords:Diels-Alder Reactions; Metathesis; Oxygen Heterocycles; Terpenes
ID Code:88002
Deposited On:26 Mar 2012 13:55
Last Modified:26 Mar 2012 13:55

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