Literature DB >> 24234019

Determining enantiomeric composition of disparlure.

J E Oliver1, R M Waters.   

Abstract

A method has been developed to convert disparlure (2-methyl-7,8-epoxyoctadecane) to the correspondingN-(α-methylbenzyl)aziridine with inversion of configuration at both the 7 and 8 positions. The diastereomeric aziridines can be separated on an efficient gas chromatography column, permitting determination of the enantiomeric constitution of the starting disparlure. As little as ca. 0.1% of the minor enantiomer can be detected.

Entities:  

Year:  1995        PMID: 24234019     DOI: 10.1007/BF02036651

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


  1 in total

1.  Capture of gypsy moth,Lymantria dispar (L.), andLymantria mathura (L.) males in traps baited with disparlure enantiomers and olefin precursor in the People's Republic of China.

Authors:  T M Odell; C H Xu; P W Schaefer; B A Leonhardt; D F Yao; X D Wu
Journal:  J Chem Ecol       Date:  1992-12       Impact factor: 2.626

  1 in total
  1 in total

1.  Semiochemicals via epoxide inversion.

Authors:  J E Oliver; R M Waters; D J Harrison
Journal:  J Chem Ecol       Date:  1996-02       Impact factor: 2.626

  1 in total

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