Literature DB >> 17107057

Reaction of azetidines with chloroformates.

Monica Vargas-Sanchez1, Sami Lakhdar, François Couty, Gwilherm Evano.   

Abstract

The reaction of an azetidine with a chloroformate can give either the dealkylated heterocycle or the ring-opened product (gamma-chloroamine), which can further cyclize to the oxazinanone. A general study of this underrated reaction was conducted and revealed that azetidines can undergo smooth nucleophilic ring-opening reactions to highly functionalized gamma-chloroamines in the presence of a variety of alkyl chloroformates under mild reaction conditions. Yields are usually good, and parameters governing this reaction were evaluated. [reaction: see text].

Entities:  

Year:  2006        PMID: 17107057     DOI: 10.1021/ol062128c

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

1.  Synthesis of (+/-)- and (-)-vibralactone and vibralactone C.

Authors:  Quan Zhou; Barry B Snider
Journal:  J Org Chem       Date:  2008-09-19       Impact factor: 4.354

2.  Synthesis of tertiary alkyl fluorides and chlorides by site-selective nucleophilic ring-opening reaction of α-aryl azetidinium salts.

Authors:  Eiji Tayama; Kohei Kawai
Journal:  RSC Adv       Date:  2021-12-13       Impact factor: 3.361

3.  Preparation and Evaluation of a Novel Class of Amphiphilic Amines as Antitumor Agents and Nanocarriers for Bioactive Molecules.

Authors:  Isabella Orienti; Mirella Falconi; Gabriella Teti; Mark A Currier; Jiang Wang; Mitch Phelps; Timothy P Cripe
Journal:  Pharm Res       Date:  2016-07-25       Impact factor: 4.200

  3 in total

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