Convenient Synthesis of trans-β-Amino Carboxylic Esters with an Azetidine Skeleton via Rearrangement of β,γ-Aziridino α-amino Esters-Reference-Cited by-同舟云学术

Convenient Synthesis of trans-β-Amino Carboxylic Esters with an Azetidine Skeleton via Rearrangement of β,γ-Aziridino α-amino Esters

Published:2007-09-19 Issue:21 Volume:9 Page:4399-4402
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Kiss Loránd¹,Mangelinckx Sven¹,Fülöp Ferenc¹,De Kimpe Norbert¹

Affiliation:

1. Department of Organic Chemistry, Faculty of Bioscience Engineering, Ghent University, Coupure Links 653, B-9000 Ghent, Belgium, and Institute of Pharmaceutical Chemistry, University of Szeged, P.O. Box 427, H-6701 Szeged, Hungary

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol7020466

Reference52 articles.

1. The azetidines. Recent synthetic developments

2. (b) Moore, J. A.; Ayers, R. S. InChemistry of Heterocyclic Compounds-Small RingHeterocycles; Hassner, A., Ed.; Wiley: New York, 1983; Part 2, pp 1−217.

3. A novel synthesis of 3-aminoazetidines by ring transformation of 2-(bromomethyl)aziridines

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