Synthesis of 7E,9Z-dodecadienyl acetate, the sex pheromone ofLobesia botrana Shiff

Chrelashvili, Z. G.; Mavrov, M. V.; Dolidze, A. V.; Voronkov, A. P.; Serebryakov, É. P.

doi:10.1007/bf00704016

Search citation statements

Order By: Relevance

Paper Sections

Select...

Scheme 402

Citation Types

Supporting

Mentioning

Contrasting

Year Published

1998

Publication Types

Select...

Article1

Relationship

Self Cite0

Independent1

Authors

Journals

Cited by 1 publication

(2 citation statements)

References 24 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…Conversion into the bromide 7.103 followed by reaction with 5-(tetrahydropyranyloxy)pentylmagnesium bromide, hydrolysis and acetylation furnished the final products 7. 99 Odinokov and coworkers 126 described the synthesis of isopropyl (3E)-nona-3,8-dienoate (7.106), the key compound for a variety of pheromone components. It was used, for instance, for the synthesis of acetates 7.104 and 7.105, the pheromone components of various Lepidopteran species.…”

Section: Scheme 48mentioning

confidence: 99%

“…Chrelashvili et al 99 performed the synthesis of 7.25, the Lobesia botrana pheromone, using (3E,5Z)-1-bromoocta-3,5-diene (7.27) as the main building block. The 3E,5Z-double bond configuration was achieved by stepwise reduction of the diacetylenic alcohol 7.29 by means of LiAlH 4 reduction of the ∆ 3 bond followed by the Zn/Cu/ i-PrOH reduction of the other.…”

Section: Scheme 40mentioning

confidence: 99%

See 1 more Smart Citation