Literature DB >> 24301893

Stereoisomers and analogs of 14-methyl-1-octadecene, sex pheromone of peach leafminer moth,Lyonetia clerkella, L.

P E Sonnet1, A T Proveaux, E Adamek, H Sugie, R Sato, Y Tamaki.   

Abstract

The synthesis of the enantiomeric 14-methyl-1-octadecenes in >99% EE is described. Enantiomeric 2-methyl-1-hexanols were intermediates in the synthesis. The 1-alkene had been previously identified as the sex pheromone of the peach leafminer moth. Several closely related structures that have δ12 unsaturation are also described.

Entities:  

Year:  1987        PMID： 24301893     DOI： 10.1007/BF01880098

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


  1 in total

1.  General approach to synthesis of chiral branched hydrocarbons in high configurational purity.

Authors:  P E Sonnet
Journal:  J Chem Ecol       Date:  1984-05       Impact factor: 2.626
  1 in total
  2 in total

1.  Identification of female-produced sex pheromone from banded cucumber beetle,Diabrotica balteata leconte (Coleoptera: Chrysomelidae).

Authors:  T Chuman; P L Guss; R E Doolittle; J R McLaughlin; J L Krysan; J M Schalk; J H Tumlinson
Journal:  J Chem Ecol       Date:  1987-07       Impact factor: 2.626

2.  Enantiomers of methyl substituted analogs of (Z)-5-decenyl acetate as probes for the chirality and complementarity of its receptor inAgrotis segetum 1: Synthesis and structure-activity relationships.

Authors:  S Jönsson; T Malmström; T Liljefors; B S Hansson
Journal:  J Chem Ecol       Date:  1993-03       Impact factor: 2.626
  2 in total

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