Straightforward synthesis of novel enantiopure α-trifluoromethylated azetidine 2-carboxylic acid and homoserines.

Org Lett

Laboratoire de Chimie Biologique (LCB), EA 4505, Université de Cergy-Pontoise, 5 Mail, Gay-Lussac, Neuville sur Oise, 95000 Cergy-Pontoise Cedex, France.

Published: January 2015

The straightforward syntheses of enantiopure (2R)-2-trifluoromethyl-2-carboxyazetidine and (R)- and (S)-trifluoromethylhomoserines are reported. The key step is a Strecker-type reaction on a common chiral CF3-containing bicyclic oxazolidine intermediate obtained by a condensation reaction of (R)-phenylglycinol and ethyl-4,4,4-trifluoroacetoacetate (ETFAA).

Download full-text PDF

Source
http://dx.doi.org/10.1021/ol503448wDOI Listing

Publication Analysis

Top Keywords

straightforward synthesis
4
synthesis novel
4
novel enantiopure
4
enantiopure α-trifluoromethylated
4
α-trifluoromethylated azetidine
4
azetidine 2-carboxylic
4
2-carboxylic acid
4
acid homoserines
4
homoserines straightforward
4
straightforward syntheses
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!