Volume 26, Issue 19
Natural Products
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ChemInform Abstract: Prostaglandin Chemistry. Part 43. Studies on the Preparation of Isocarbacyclin Intermediates. Part 2.

M. KOGA

M. KOGA

Iwakuni Pharm. Fact., Chem. Manuf. Plant Teijin Ltd., Iwakuni, Yamaguchi 740, Japan

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H. KAGEYAMA

H. KAGEYAMA

Iwakuni Pharm. Fact., Chem. Manuf. Plant Teijin Ltd., Iwakuni, Yamaguchi 740, Japan

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T. TANAKA

T. TANAKA

Iwakuni Pharm. Fact., Chem. Manuf. Plant Teijin Ltd., Iwakuni, Yamaguchi 740, Japan

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T. FUJII

T. FUJII

Iwakuni Pharm. Fact., Chem. Manuf. Plant Teijin Ltd., Iwakuni, Yamaguchi 740, Japan

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First published: May 9, 1995

Abstract

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ChemInform Abstract

2,2,2-Trifluoroethanol is found to be the most effective proton source for the reductive cyclization of the aldehyde (I) with lithium naphthalene leading to the precursors (II) and (III) of the prostacyclin mimic isocarbacyclin.

chemical structure image

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