Highly Stereodivergent Approach to Both Enantiomers of 4-Substituted β-Lactams via Diastereofacially Controlled Addition of Enolates oft-Butyl Acetate to a Chiral Imine-Reference-Cited by-同舟云学术

Highly Stereodivergent Approach to Both Enantiomers of 4-Substituted β-Lactams via Diastereofacially Controlled Addition of Enolates oft-Butyl Acetate to a Chiral Imine

Published:1992-07 Issue:7 Volume:21 Page:1349-1352
ISSN:0366-7022
Container-title:Chemistry Letters
language:en
Short-container-title:Chem. Lett.

Author:

Shimizu Makoto,Ukaji Yutaka,Tanizaki Junko,Fujisawa Tamotsu

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/cl/21/7/21_7_1349/_pdf

Reference22 articles.

1. Recent Developments in the Field of β-Lactam Antibiotics

2. Synthesis of Carbapenem Antibiotics

3. A stereocontrolled synthesis of (+)-thienamycin

4. The penems, a new class of .beta.-lactam antibiotics. 5. Total synthesis of racemic 6-.alpha.-hydroxyethylpenemcarboxylic acids

5. A stereodivergent construction of β-lactam skeletons via condensation of ester enolates and a chiral imine

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