Diastereoselective ring cleavage of azetidines with cyanogen bromide-Reference-Cited by-同舟云学术

Diastereoselective ring cleavage of azetidines with cyanogen bromide

Published:2022-03 Issue: Volume:94 Page:153710
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Raulin Melvin^ORCID,Drouillat Bruno,Marrot Jérome,Couty François,Wright Karen^ORCID

Funder

Ministère de l'Enseignement supérieur, de la Recherche et de l'Innovation

Centre National de la Recherche Scientifique

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference16 articles.

1. F. Couty, “Synthesis of Azetidines”, in Science of Synthesis: Houben-Weyl Methods of Molecular Transformations (Ed.: D. Enders), Georg Thieme Verlag: New York, 2009; Vol. 40a, pp. 773–817.

2. Ring‐opening of azetidiniums by nucleophiles. Synthesis of polysubstituted linear amines

3. Recent advances in synthetic facets of immensely reactive azetidines

4. Reaction of Azetidines with Chloroformates

5. BF3·OEt2-Mediated Highly Regioselective SN2-Type Ring-Opening of N-Activated Aziridines and N-Activated Azetidines by Tetraalkylammonium Halides

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