Synthesis of Enantiomerically Pure Aziridine-2-imides by Cyclization of Chiral 3‘-Benzyloxyamino Imide Enolates-Reference-Cited by-同舟云学术

Synthesis of Enantiomerically Pure Aziridine-2-imides by Cyclization of Chiral 3‘-Benzyloxyamino Imide Enolates

Published:1997-12-01 Issue:26 Volume:62 Page:9148-9153
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Bongini Alessandro¹,Cardillo Giuliana¹,Gentilucci Luca¹,Tomasini Claudia¹

Affiliation:

1. Dipartimento di Chimica “G. Ciamician”, Università di Bologna, via Selmi 2, 40126 Bologna, Italy

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo971254e

Reference33 articles.

1. (a) Fanta, P. E.Heterocyclic Compounds with Three- and Four-memberd Rings; Weissemberg, A., Ed.; Wiley Intrerscience: NewYork, 1964, Part 1, p 524.

2. Chiral Aziridines—Their Synthesis and Use in Stereoselective Transformations

3. Mono-osmylation of dehydroamino acid dienes: synthesis of dehydroamino acids related to the azinomycins

4. Total synthesis of natural (+)-FR900482. 1. Synthetic and end-game strategies

5. A new access to chiral aziridines by enzymatic transesterification of meso-bis(acetoxymethyl)aziridines

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