Synthesis of the enantiomers of 1,7-dioxaspiro[5.5]undecane and 4-hydroxy 1,7-dioxaspiro[5.5]undecane, the components of the olive fly pheromone
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference14 articles.
1. Identification and synthesis of the major sex pheromone of the olive fly (Dacus oleae)
2. A new route to spiro-ketals using the Horner-Wittig reaction of 2-diphenylphosphinoxy cyclic ethers
3. Synthesis of three stereoisomeric forms of 2,8-dimethyl-1,7-dioxaspiro[5.5]undecane, the main component of the cephalic secretion of andrena wilkella
4. 1,7-Dioxaspiro[5.5]undecanes. An excellent system for the study of stereoelectronic effects (anomeric and exo-anomeric effects) in acetals
5. Isolation and synthesis of 3- and 4-hydroxy-1,7-dioxaspiro[5.5]undecanes from the olive fly (Dacus oleae)
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