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Asymmetric synthesis with chiral hydrogenolysable amines, ω-imino esters reduction: A diastereoselective route to ω-alkyl lactams

DOI: 10.1016/S0040-4039(00)74246-8

Source and publish data:

Tetrahedron Letters p. 4307 - 4310 (1992)

Update date:2022-09-26

Topics: Characterization   Isolation and Purification   Removal of chiral auxiliary   Diastereoselective Reduction  

Authors:

MarxMarx

El BouzEl Bouz

CelerierCelerier

LhommetLhommet

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Article abstract of DOI:10.1016/S0040-4039(00)74246-8

Chiral methylbenzylamine is used to prepare ω-amino esters which are then transformed into ω-alkyl lactams with good diastereoselectivity.

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Full text of DOI:10.1016/S0040-4039(00)74246-8

Products guided by the article

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Cas No:321567-00-4

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