64275-76-9Relevant articles and documents
Selective conversion of enol ethers into alcohols in the presence of alkenes using Hg(OAc)2-NaBH4
Crouch, R. David,Mehlmann, John F.,Herb, Brian R.,Mitten, Jeffrey V.,Dai, H. George
, p. 559 - 561 (2007/10/03)
Alkyl enol ethers derived from aldehydes undergo selective oxymercuration-demercuration with aqueous Hg(OAc)2-NaBH4 in the presence of an alkene in good to excellent yield. This method allows the survival of mono-, trans and cis di-, and tri-substituted alkenes as well as cyclic alkenes.
Synthesis of (Z)-6-heneicosen-11-one, (+/-)(Z)-14-methyl-8-hexadecen-1-ol and (+/-)-5,6-dehydrosenedigitalene
Sharma, M. L.,Verma, Sadhana,Chand, Tek
, p. 1030 - 1034 (2007/10/03)
Three naturally occurring compounds (Z)-6-heneicosen-11-one (1), (+/-)-(Z)-14-methyl-8-hexadecen-1-ol (2) and (+/-)-5,6-dehydrosenedigitalene (3) have been synthesised using lithium tetrachlorocuperate catalysed coupling reaction.
INSECT PHEROMONES AND THEIR ANALOGUES XXXI. SYNTHESIS OF DEC-5Z-EN-1-YL ACETATE AND HENEICOS-6Z-EN-11-ONE FROM A FUNCTIONALLY DIFFERENTIATED PRODUCT OF THE OZONOLYSIS OF CYCLOPENTENE
Odinokov, V. N.,Akhmetova, V. R.,Khasanov, Kh. D.,Abduvakhabov, A. A.,Tolstikov, O. A.
, p. 497 - 499 (2007/10/02)
Dec-5Z-en-1-yl acetate and heneicos-6Z-en-11-one - pheromones of insects of the genera Agrotis and Orgyia, respectively - have been synthesized from a product of the functionally differentiated ozonolysis of cyclopentene.