64308-75-4Relevant academic research and scientific papers
COMPOSITION FOR ATTRACTING MALE BLUEBERRY SPANWORM MOTH
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Paragraph 0060, (2015/02/25)
A composition that includes: Z,Z-(3R,4S)-cis-3,4-epoxy-6,9-heptadecadiene; and Z,Z,Z-3,6,9-heptadecatriene, where the Z,Z-(3R,4S)-cis-3,4-epoxy-6,9-heptadecadiene and the Z,Z,Z-3,6,9-heptadecatriene are present in a ratio of between 5:1 (by mass) and about 20:1 (by mass). The composition may be for attracting a male blueberry spanworm moth. Use of a composition that includes Z,Z-(3R,4S)-cis-3,4-epoxy-6,9-heptadecadiene and Z,Z,Z-3,6,9-heptadecatriene for attracting male blueberry spanworm. A method of attracting male blueberry spanworm moths that includes placing a composition comprising Z,Z-(3R,4S)-cis-3,4-epoxy-6,9-heptadecadiene and Z,Z,Z-3,6,9-heptadecatriene suitably close to a field of having the male blueberry spanworm moths.
Formal synthesis of (+)-isolaurepinnacin
Suzuki, Toshio,Matsumura, Ryuji,Oku, Ken-ichi,Taguchi, Keiichi,Hagiwara, Hisahiro,Hoshi, Takashi,Ando, Masayoshi
, p. 65 - 67 (2007/10/03)
The stereoselective formal synthesis of (+)-isolaurepinnacin is described. The required key oxepene skeleton possessing cis-oriented alkyl substituents at the α,ω-positions was stereoselectively constructed via the cyclization of the corresponding hydroxy epoxide promoted by the (Bu3Sn)2O/Zn(OTf)2 system.
Stereoselective Acetalization of 1,1- and 1,2-Disubstituted Diols as Common Principle in the Synthesis of the Enantiomers of the Bicyclic Acetal Pheromones endo- and exo-Brevicomin and Frontalin
Wershofen, Stefan,Classen, Arnold,Scharf, Hans-Dieter
, p. 9 - 18 (2007/10/02)
The acetalization of the 1,1- and 1,2-disubstituted diols 14-19 with the keto compounds 20 and 21 has been investigated.The substitution pattern of the used diols shows great influence on the stereochemistry of the obtained dioxolanes 22-27 (mixtures of d
