A short and efficient synthesis of renealtins A and B

Sabitha, Gowravaram ; Yadagiri, K. ; Yadav, J. S. (2007) A short and efficient synthesis of renealtins A and B Tetrahedron Letters, 48 (45). pp. 8065-8068. 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.2007.09.025

Abstract

The total syntheses of the first examples of diarylheptanoid natural products, renealtins A (1) and B (2), isolated from Renealmia exaltata are described, utilizing a δ-lactone intermediate 9. The key reactions involved are asymmetric dihydroxylation and oxy-Michael addition.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
Keywords:Natural Products; Diarylheptanoids; Tetrahydrofuran Ring; Oxy-Michael; Dihydroxylation
ID Code:63069
Deposited On:28 Sep 2011 03:35
Last Modified:28 Sep 2011 03:35

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