Volume 31, Issue 23
Natural Products
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ChemInform Abstract: Enzyme-Assisted Asymmetric Total Synthesis of (-)-Podophyllotoxin and (-)-Picropodophyllin.

David B. Berkowitz

David B. Berkowitz

Dep. Chem., Univ. Nebr., Lincoln, NE 68588, USA

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Sungjo Choi

Sungjo Choi

Dep. Chem., Univ. Nebr., Lincoln, NE 68588, USA

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Jun-Ho Maeng

Jun-Ho Maeng

Dep. Chem., Univ. Nebr., Lincoln, NE 68588, USA

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First published: 08 June 2010

Abstract

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

ChemInform Abstract

The key steps in the synthesis of the title compounds are stereoselective formation of the meso diester (V), enzymatic desymmetrization of the meso diacetate (VI), and stereoselective introduction of the (3,4,5-trimethoxy)phenyl group.

chemical structure image

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