Volume 29, Issue 1
Natural Products
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ChemInform Abstract: Hemisynthesis of Rhazinilam Analogues: Structure—Activity Relationships on Tubulin-Microtubule System.

B. DAVID

B. DAVID

Inst. Chim. Subst. Nat., CNRS, F-91198 Gif-sur-Yvette, Fr.

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T. SEVENET

T. SEVENET

Inst. Chim. Subst. Nat., CNRS, F-91198 Gif-sur-Yvette, Fr.

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O. THOISON

O. THOISON

Inst. Chim. Subst. Nat., CNRS, F-91198 Gif-sur-Yvette, Fr.

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K. AWANG

K. AWANG

Inst. Chim. Subst. Nat., CNRS, F-91198 Gif-sur-Yvette, Fr.

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M. PAIS

M. PAIS

Inst. Chim. Subst. Nat., CNRS, F-91198 Gif-sur-Yvette, Fr.

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M. WRIGHT

M. WRIGHT

Inst. Chim. Subst. Nat., CNRS, F-91198 Gif-sur-Yvette, Fr.

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D. GUENARD

D. GUENARD

Inst. Chim. Subst. Nat., CNRS, F-91198 Gif-sur-Yvette, Fr.

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First published: 24 June 2010

Abstract

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ChemInform Abstract

A series of rhazinilam analogues, e.g. (IV)—(VII), is prepared by conventional procedures to delineate some molecular features necessary for biological activity. However, none of these analogues have a higher activity than rhazinilam (III). In the course of this study, the formation of (III) from (I) is reexamined. The isolation of N-oxide (II) leads to a new proposal concerning the mechanism of this transformation (no yields given).

chemical structure image

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