Halogenative Allylation and Reduction of Aromatic Acetals by Double Substitution of Alkoxyl Groups in Acetal

DOI: 10.1246/bcsj.64.1410

Source and publish data:

Bulletin of the Chemical Society of Japan p. 1410 - 1412 (1991)

Update date:2022-07-29

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Authors:

Oriyama, Takeshi

Iwanami, Katsuyuki

Tsukamoto, Kazuhisa

Ichimura, Yuichi

Koga, Gen

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Article abstract of DOI:10.1246/bcsj.64.1410

In the presence of excessive amount of acetyl halide along with a catalytic amount of tin(II) halide, aromatic acetals react with allyltrimethylsilane or triethylsilane to give α-allylbenzyl halides or benzyl halides, respectively, in good to excellent yields.

Full text of DOI:10.1246/bcsj.64.1410

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