Asymmetric synthesis of 2-substituted-3-aminocarbonyl propionic acid.

DOI: 10.1248/cpb.37.2200

Source and publish data:

Chemical and pharmaceutical bulletin p. 2200 - 2203 (1989)

Update date:2022-08-03

Topics:

Authors:

Nishi Nishi

Sakurai Sakurai

Sato Sato

Kataoka Kataoka

Morisawa

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Article abstract of DOI:10.1248/cpb.37.2200

An asymmetric synthetic route to 2-substituted-3-aminocarbonyl propionic acid, which is the significant component of low-molecular-weight renin inhibitors, is described. The key step of this synthesis is diastereoselective alkylation by using chiral oxazo

Full text of DOI:10.1248/cpb.37.2200

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