Literature DB >> 24414583

Synthesis of (±)-10-methyl-1-dodecanol acetate, the chiral component of the smaller tea tortrix moth (Adoxophyes sp.), with an option for asymmetric induction.

P E Sonnet1, R R Heath.   

Abstract

A new route to (±)-10-methyl-1-dodecanol acetate, a minor component of the smaller tea tortrix moth (Adoxophyes sp.), is described. An optional sequence that permits the generation of the chiral center with enantiomeric excesses (ee's) as high as 74% (R) or 80% (S) employing the available (S)-(-)-prolinol as a chiral auxiliary may be included. High-performance liquid chromatography of diastereomeric intermediates allows preparation of products with greater ee's.

Entities:  

Year:  1982        PMID: 24414583     DOI: 10.1007/BF00984004

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


  1 in total

1.  The synthesis of the optically active form of the C-18 Cecropia juvenile hormone.

Authors:  P Loew; W S Johnson
Journal:  J Am Chem Soc       Date:  1971-07-28       Impact factor: 15.419

  1 in total

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