Asymmetric synthesis of unnatural (Z,Z,E)-octadecatrienoid and eicosatrienoid by lipoxygenase-catalyzed oxygenation

Nanda, S. ; Yadav, J. S. (2003) Asymmetric synthesis of unnatural (Z,Z,E)-octadecatrienoid and eicosatrienoid by lipoxygenase-catalyzed oxygenation Tetrahedron: Asymmetry, 14 (13). pp. 1799-1806. ISSN 0957-4166

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

Related URL: http://dx.doi.org/10.1016/S0957-4166(03)00369-0

Abstract

The asymmetric synthesis of unnatural 13-hydroxy-(6Z,9Z,11E,13S)-octadecatrienoid and 15-hydroxy-(8Z,11Z,13E,15S)-eicosatrienoid is described using a biomimetic oxidation route. The main highlights of this synthesis are the asymmetric hydroxylation of the substrate with soybean lipoxygenase and cis selective Wittig olefination.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
ID Code:58837
Deposited On:02 Sep 2011 03:18
Last Modified:02 Sep 2011 03:18

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