Dialkyl and diaryl boron halides: reductive opening of benzylidene acetals
- 1 June 1990
- journal article
- Published by Canadian Science Publishing in Canadian Journal of Chemistry
- Vol. 68 (6) , 897-902
- https://doi.org/10.1139/v90-141
Abstract
Dimethylboron bromide or diphenylboron bromide can be used in combination with borane to achieve the regiocontrolled conversion of benzylidene acetals to their corresponding hydroxy benzyl ethers with moderate to high yields. Keywords: dimethylboron bromide, diphenylboron bromide, reductive opening, benzylidene, acetals.Keywords
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