Literature DB >> 19284796

Expedient preparation of all isomers of 2-aminocyclobutanecarboxylic acid in enantiomerically pure form.

Carlos Fernandes1, Elisabeth Pereira, Sophie Faure, David J Aitken.   

Abstract

A short, convenient, gram scale protocol has been established to allow facile access to all four stereoisomers of 2-aminocyclobutanecarboxylic acid, each in enantiomerically pure form (ee >99%). Starting from the readily available cis racemate, the procedure combines efficient alpha-phenylethylamine derivative resolution and controlled cis-to-trans epimerization procedures, and proceeds with invariably high yields.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19284796     DOI: 10.1021/jo900175p

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

1.  Efficient regio- and stereoselective access to novel fluorinated β-aminocyclohexanecarboxylates.

Authors:  Loránd Kiss; Melinda Nonn; Reijo Sillanpää; Santos Fustero; Ferenc Fülöp
Journal:  Beilstein J Org Chem       Date:  2013-06-17       Impact factor: 2.883

2.  Syntheses of four enantiomers of 2,3-diendo- and 3-endo-aminobicyclo[2.2.2]oct-5-ene-2-exo-carboxylic acid and their saturated analogues.

Authors:  Márta Palkó; Mikko M Hänninen; Reijo Sillanpää; Ferenc Fülöp
Journal:  Molecules       Date:  2013-12-06       Impact factor: 4.411

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.