An Efficient and Solvent-Free Synthesis of Mixed Ortho Esters
Author(s)
L. Cosgrove, Kelly
P. McGeary, Ross
Griffith University Author(s)
Year published
2008
Metadata
Show full item recordAbstract
Primary, secondary and electron-deficient tertiary alcohols react rapidly with ketene dimethyl acetal to form mixed ortho esters, without catalysts and under solvent-free conditions. 1,2-Diols yield bis(mixed ortho esters), rather than cyclic ortho esters.Primary, secondary and electron-deficient tertiary alcohols react rapidly with ketene dimethyl acetal to form mixed ortho esters, without catalysts and under solvent-free conditions. 1,2-Diols yield bis(mixed ortho esters), rather than cyclic ortho esters.
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Journal Title
Synlett
Volume
2008
Issue
16
Subject
Organic Chemical Synthesis
Medicinal and Biomolecular Chemistry
Organic Chemistry