Reaktionen mit Aziridinen, 47. Mitt. Regiospezifität und Stereoselektivität der säurekatalysierten Alkoholyse von cis-2-Benzyl-3-phenyl-1-phenylsulfonylaziridin-Reference-Cited by-同舟云学术

Reaktionen mit Aziridinen, 47. Mitt. Regiospezifität und Stereoselektivität der säurekatalysierten Alkoholyse von cis-2-Benzyl-3-phenyl-1-phenylsulfonylaziridin

Published:1989 Issue:5 Volume:322 Page:277-279
ISSN:0365-6233
Container-title:Archiv der Pharmazie
language:de
Short-container-title:Arch. Pharm. Pharm. Med. Chem.

Author:

Stamm Helmut,Speth Dieter

Publisher

Wiley

Subject

Drug Discovery,Pharmaceutical Science

Reference11 articles.

1. Reactions with aziridines, 46. Ring opening of stilbene imines by thiophenolate

2. Reactions with Aziridines, XXXII[1]. Mechanistic Aspects in Nucleophilic Opening of Three-Membered Rings. Alcoholyses of Activated Aziridines

3. Reactions with aziridines. 43. Reactivity difference of cis-trans pairs: different behavior of stilbene oxides and activated stilbene imines

4. Nucleophilic cleavage of 2,2-dimethylaziridines: competition between SN2 and postulated “SET” mechanism.

5. Reactions with Aziridines, 37 [1]. N,N'-Substituted 1,1-Dimethylethylenediamines by Highly Regioselective Ring Opening of Activated 2,2-Dimethylaziridines through Aliphatic Amines

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