Kinetically Controlled Regiospecific Silylation of Polyols via Dibutylstannanediyl Acetals

DOI: 10.1039/c39940001373

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 1373 - 1374 (1994)

Update date:2022-09-26

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Authors:

Leigh, David A.

Martin, Richard P.

Smart, John P.

Truscello, Ada M.

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Article abstract of DOI:10.1039/c39940001373

A general procedure is described whereby the tert-butyldimethylsilylation of unsymmetrical 1,2- and 1,3-diols via their dibutylstannanediyl derivatives occurs regiospecifically at the primary hydroxy group under neutral conditions; six-membered ring aceta

Full text of DOI:10.1039/c39940001373

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