Syntheses of both enantiomers of 1,7-dioxaspiro[5.5]undecane: Pheromone components of the olive fruit-fly Dacus oleae from a new chiral intermediate, the (S(s))-2-(p-tolylsulfinyl)prop-2-en-1-ol

Synthesis

Volumn , Issue 5, 1999, Pages 783-786

  Hayes, Patricia ^a   Maignan, Christian ^a  

^a UNIVERSITÉ DU MAINE   (France)

Author keywords

(Ss) 2 (p tolylsulfinyl)prop 2 en 1 ol; Chiral 1,7 dioxaspiro 5.5 undecane; Chiral sulfinyl heterodiene; Hetero Diels Alder reaction; Insect pheromone

Indexed keywords

DECANE; PHEROMONE; SULFOXIDE;

ARTICLE; CHEMICAL REACTION; CHIRALITY; DESULFURIZATION; DROSOPHILA; ENANTIOMER; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; POLYMERIZATION; SYNTHESIS;

EID: 0032941403     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1999-3467     Document Type: Article

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