Issue 3, 1990

Perkin communications. 4,4′-Dimethoxytrityl and 4-monomethoxytrityl tetrafluoroborate: convenient reagents for the protection of primary alcohols including sugars

Abstract

In a non-donor solvent (e.g. acetonitrile) and in the presence of 2,6-di-t-butyl-4-methylpyridine, the readily prepared 4-methoxytrityl tetrafluoroborate (3) and 4,4′-dimethoxytrityl tetrafluoroborate (2) are highly effective reagents for the methoxytritylation and dimethoxytritylation, respectively, of primary alcohols including sugars.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1990, 803-805

Perkin communications. 4,4′-Dimethoxytrityl and 4-monomethoxytrityl tetrafluoroborate: convenient reagents for the protection of primary alcohols including sugars

C. Bleasdale, S. B. Ellwood and B. T. Golding, J. Chem. Soc., Perkin Trans. 1, 1990, 803 DOI: 10.1039/P19900000803

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