Enantiomers of cis- and trans-3-(4-propyl-cyclopent-2-enyl) propyl acetate. A study on the bioactive conformation and chiral recognition of a moth sex pheromone component

Bioorganic and Medicinal Chemistry

Volumn 5, Issue 12, 1997, Pages 2173-2183

  Gustavsson, Anna Lena ^a   Larsson, Mattias C ^a   Hansson, Bill S ^a   Liljefors, Tommy ^b  

^a LUND UNIVERSITY   (Sweden)

^b UNIVERSITY OF COPENHAGEN   (Denmark)

Author keywords

Agrotis segetum; Chiral recognition; Pheromone analogues; Single cell recordings; Structure activity

Indexed keywords

3 (4 PROPYLCYCLOPENT 2 ENYL)PROPYL ACETATE; SEX PHEROMONE; UNCLASSIFIED DRUG;

ARTICLE; CHIRALITY; DRUG CONFORMATION; DRUG SYNTHESIS; ENANTIOMER; NONHUMAN; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; OLFACTORY RECEPTOR; STEREOCHEMISTRY; STEREOISOMERISM;

ACETATES; ANIMALS; ELECTROPHYSIOLOGY; ISOMERISM; MALE; MODELS, CHEMICAL; MODELS, MOLECULAR; MOTHS; SENSE ORGANS; SEX ATTRACTANTS;

EID: 0031439072     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0968-0896(97)00162-4     Document Type: Article

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