Literature DB >> 24227410

Semiochemicals via epoxide inversion.

J E Oliver1, R M Waters, D J Harrison.   

Abstract

A sequence of reactions is presented for inverting the configurations of both epoxide carbons in 1,2-disubstituted epoxides. As examples, (+)-disparlure was converted to its enantiomer, (-)-disparlure, andexo-endo conversion of a cyclohexene oxide was demonstrated.

Entities:  

Year:  1996        PMID: 24227410     DOI: 10.1007/BF02055099

Source DB:  PubMed          Journal:  J Chem Ecol        ISSN: 0098-0331            Impact factor:   2.626


  2 in total

1.  Determining enantiomeric composition of disparlure.

Authors:  J E Oliver; R M Waters
Journal:  J Chem Ecol       Date:  1995-02       Impact factor: 2.626

2.  Potent sex attractant of the gypsy moth: its isolation, identification, and synthesis.

Authors:  B A Bierl; M Beroza; C W Collier
Journal:  Science       Date:  1970-10-02       Impact factor: 47.728

  2 in total
  1 in total

1.  Enzymatic synthesis and chemical inversion provide both enantiomers of bioactive epoxydocosapentaenoic acids.

Authors:  Maris A Cinelli; Jun Yang; Amy Scharmen; Joey Woodman; Lalitha M Karchalla; Kin Sing Stephen Lee
Journal:  J Lipid Res       Date:  2018-09-12       Impact factor: 5.922

  1 in total

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