NOVEL HYDROXYMETHYLATION OF ARYL BROMIDES BY MEANS OF ORGANOTIN REAGENTS

DOI: 10.1246/cl.1985.997

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Chemistry Letters p. 997 - 998 (1985)

Update date:2022-08-11

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Authors:

Kosugi, Masanori

Sumiya, Takashi

Ohhashi, Kenji

Sano, Hiroshi

Migita, Toshihiko

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Article abstract of DOI:10.1246/cl.1985.997

Direct transformation of aryl bromides to benzylic alcohols by means of hydroxymethyltributyltin in the presence of palladium complex was attained in moderate yields, although the catalytic efficiencies were rather low, and the reaction could not be applied to aryl bromides having strong electron-withdrawing group.These problems were solved by using the trimethylsilyl-protected tin compound.

Full text of DOI:10.1246/cl.1985.997

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NOVEL HYDROXYMETHYLATION OF ARYL BROMIDES BY MEANS OF ORGANOTIN REAGENTS

DOI: 10.1246/cl.1985.997

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Authors:

Article abstract of DOI:10.1246/cl.1985.997

Full text of DOI:10.1246/cl.1985.997

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