Stereoselective Synthesis of Chiral 4-(1-Chloroalkyl)-β-Lactams Starting from Amino Acids and Their Transformation into Functionalized Chiral Azetidines and Pyrrolidines-Reference-Cited by-同舟云学术

Stereoselective Synthesis of Chiral 4-(1-Chloroalkyl)-β-Lactams Starting from Amino Acids and Their Transformation into Functionalized Chiral Azetidines and Pyrrolidines

Published:2010-08-12 Issue:17 Volume:75 Page:5934-5940
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Dekeukeleire Stijn¹,D’hooghe Matthias¹,Törnroos Karl W.²,De Kimpe Norbert¹

Affiliation:

1. Department of Organic Chemistry, Faculty of Bioscience Engineering, Ghent University, Coupure links 653, B-9000 Ghent, Belgium

2. Department of Chemistry, University of Bergen, Allégt. 41, 5007 Bergen, Norway

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo101220q

Reference40 articles.

1. Enantioselective Staudinger Synthesis of β-Lactams Catalyzed by a Planar-Chiral Nucleophile

2. Catalytic, Asymmetric Synthesis of β-Lactams

3. The Development of the First Catalyzed Reaction of Ketenes and Imines: Catalytic, Asymmetric Synthesis of β-Lactams

4. Asymmetric Synthesis of β-Lactams by Staudinger Ketene-Imine Cycloaddition Reaction

5. Advances in the Catalytic, Asymmetric Synthesis of β-Lactams

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