Regioselective reductive ring opening of cyclic 1,2- and 1,3-benzylidene acetals

DOI: 10.1246/cl.1998.1273

Source and publish data:

Chemistry Letters p. 1273 - 1274 (1998)

Update date:2022-08-29

Topics:

Authors:

Chandrasekhar

Ravindra Reddy

Raji Reddy

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Article abstract of DOI:10.1246/cl.1998.1273

A combination of polymethylhydrosiloxane (PMHS) and AlCl₃ was found to be a superior hydride source for reductive ring opening of cyclic benzylidene acetals of both 1,2- and 1,3-diols.

Full text of DOI:10.1246/cl.1998.1273

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