Your browser doesn't support javascript.
loading
Lewis Acid-Catalyzed Diastereoselective Synthesis of Multisubstituted N-Acylaziridine-2-carboxamides from 2 H-Azirines via Joullié-Ugi Three-Component Reaction.
Angyal, Anikó; Demjén, András; Wéber, Edit; Kovács, Anita K; Wölfling, János; Puskás, László G; Kanizsai, Iván.
Afiliação
  • Angyal A; AVIDIN Ltd. , Alsó kiköto sor 11/D , Szeged H-6726 , Hungary.
  • Demjén A; Department of Organic Chemistry , University of Szeged , Dóm tér 8 , Szeged H-6720 , Hungary.
  • Wéber E; AVIDIN Ltd. , Alsó kiköto sor 11/D , Szeged H-6726 , Hungary.
  • Kovács AK; Department of Organic Chemistry , University of Szeged , Dóm tér 8 , Szeged H-6720 , Hungary.
  • Wölfling J; SZTE-MTA Lendület Foldamer Research Group, Institute of Pharmaceutical Analysis , University of Szeged , Somogyi u. 4 , Szeged H-6720 , Hungary.
  • Puskás LG; Department of Medical Chemistry , University of Szeged , Dóm tér 8 , Szeged 6720 , Hungary.
  • Kanizsai I; Department of Organic Chemistry , University of Szeged , Dóm tér 8 , Szeged H-6720 , Hungary.
J Org Chem ; 83(7): 3570-3581, 2018 04 06.
Article em En | MEDLINE | ID: mdl-29498845
ABSTRACT
A ZnCl2-catalyzed diastereoselective Joullié-Ugi three-component reaction from 2 H-azirines, isocyanides, and carboxylic acids was established. The protocol allows the preparation of highly and diversely functionalized N-acylaziridine-2-carboxamide derivatives in up to 82% isolated yields. Moreover, the applicability of N-acylaziridines is demonstrated through a variety of transformations.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article