Ene preference in the reaction of allenylmethylsilanes with hetero-double bonds mediated by a Lewis acid

DOI: 10.1016/0022-328X(95)00306-B

Source and publish data:

Journal of Organometallic Chemistry p. 155 - 158 (1995)

Update date:2022-08-30

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Authors:

Hojo, Makoto

Murakami, Chikara

Aihara, Hidenori

Tomita, Kyoji

Miura, Katsukiyo

Hosomi, Akira

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Article abstract of DOI:10.1016/0022-328X(95)00306-B

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

Full text of DOI:10.1016/0022-328X(95)00306-B

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