76524-56-6Relevant articles and documents
Diene compound and process for producing the same
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, (2008/06/13)
The invention provides a chain diene compound with desirable regioselectivity, in the presence of a specific ruthenium compound. This chain diene compound is a promising raw material for terpene. It has a structure represented by the general formula (IX): wherein R1represents H, a C1-C6alkyl group which may be substituted or a C2-C6alkenyl group which may be substituted, R2represents a phenyl group which may have a C1-C4alkyl group or a C1-C12acyloxy group which may have a phenyl group or a naphthyl group, or a benzyl group or R2is a hydroxy group which reversibly forms an aldehyde group through shifting of the position of the double bond adjacent to said hydroxy group. The chain diene compound is produced by reacting 2-substituted-1,3-butadienes with terminal olefins in the presence of a ruthenium compound in a hydrophilic solvent. Further, the above method provides an inexpensive process for preparing a mild fragrant component and a perfume composition, such as 4-methyl-5-hexen-1-al and 4-vinyl-8-methyl-7-nonenal.
Oxovanadium-induced oxidative desilylation of allylic and benzylic silanes
Fujii, Takashi,Hirao, Toshikazu,Ohshiro, Yoshiki
, p. 5601 - 5604 (2007/10/02)
Cinnamyltrimethylsilane underwent desilylation via one-electron oxidation with VO(OEt)Cl2, which was applied to the cross-coupling with the less oxidizable allylic silanes to give the corresponding 1,5-hexadienes. Chlorination or aromatization
Application of Indium Ate Complexes to Synthetic Chemistry. Selective Conjugate Addition to Enones and Coupling with Allylic Halides
Araki, Shuki,Shimizu, Toshio,Jin, Shun-Ji,Butsugan, Yasuo
, p. 824 - 825 (2007/10/02)
Tetraorganoindium ate complexes, prepared by the addition of organolithium reagents to trialkylindium, reacted with α,β-unsaturated ketones in a 1,4-addition fashion; allylic indates derived from allylic indium sesquihalides coupled with allylic halides regio- and stereo-specifically to give high yields of hed-to-tail 1,5-dienes.