131510-05-9Relevant articles and documents
Ene preference in the reaction of allenylmethylsilanes with hetero-double bonds mediated by a Lewis acid
Hojo, Makoto,Murakami, Chikara,Aihara, Hidenori,Tomita, Kyoji,Miura, Katsukiyo,Hosomi, Akira
, p. 155 - 158 (1995)
Methylthio- and methoxy-substituted allenylmethylsilanes, a kind of allylsilanes, undergo the ene-type reaction, not the usual allylsilane-type reaction accompanying by desilylation, with carbonyl and azo compounds mediated by a Lewis acid.The correspondi
Reactions of 1,2-Propadienyl Sulfides with Aldehydes and Acetals Catalyzed by BF3*OEt2
Narasaka, Koichi,Shibata, Takanori,Hayashi, Yujiro
, p. 2825 - 2830 (2007/10/02)
Ene reaction proceeds between 1-alkyl-1,2-propadienyl sulfides and aldehydes in the presence of BF3*OEt2 to afford 1,3-dienes possessing an alkylthio group.On the other hand, the reactions of 1-silyl-1,2-propadienyl sulfides with aldehydes or their dimeth
Ene Reaction of Allenyl Sulfides with Aldehydes and Schiff's Bases Catalyzed by Lewis Acids
Hayashi, Yujiro,Shibata, Takanori,Narasaka, Koichi
, p. 1693 - 1696 (2007/10/02)
Ene reaction proceeds between α-alkyallenyl sulfides and enophiles such as aldehydes and Schiff's bases in the presence of Lewis acid to afford various 1,3-dienes.