Volume 25, Issue 40
Preparative Organic Chemistry
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ChemInform Abstract: Stereoselective Reactions. Part 22. Design and Synthesis of Chiral Chelated Lithium Amides for Enantioselective Reactions.

R. SHIRAI

R. SHIRAI

Fac. Pharm. Sci., Univ. Tokyo, Bunkyo, Tokyo 113, Japan

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K. AOKI

K. AOKI

Fac. Pharm. Sci., Univ. Tokyo, Bunkyo, Tokyo 113, Japan

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D. SATO

D. SATO

Fac. Pharm. Sci., Univ. Tokyo, Bunkyo, Tokyo 113, Japan

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H.-D. KIM

H.-D. KIM

Fac. Pharm. Sci., Univ. Tokyo, Bunkyo, Tokyo 113, Japan

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M. MURAKATA

M. MURAKATA

Fac. Pharm. Sci., Univ. Tokyo, Bunkyo, Tokyo 113, Japan

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T. YASUKATA

T. YASUKATA

Fac. Pharm. Sci., Univ. Tokyo, Bunkyo, Tokyo 113, Japan

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K. KOGA

K. KOGA

Fac. Pharm. Sci., Univ. Tokyo, Bunkyo, Tokyo 113, Japan

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First published: October 4, 1994

Abstract

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ChemInform Abstract

Starting from the phenylglycine derivative (I) a variety of optically active amines such as (VI) are prepared as precursors of chelated lithium amides possessing an additional nitrogen ligation site.

chemical structure image

    The full text of this article hosted at iucr.org is unavailable due to technical difficulties.