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Merck

A convenient synthesis of glycosyl chlorides from sugar hemiacetals using triphosgene as the chlorine source.

Carbohydrate research (2000-11-10)
R M Cicchillo, P Norris
RÉSUMÉ

Treating partially protected sugar hemiacetals with triphosgene in THF results in the formation of glycosyl chlorides. The method is compatible with acid-sensitive isopropylidene protecting groups in the hemiacetal substrates.

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Sigma-Aldrich
Triphosgene, reagent grade, 98%
Sigma-Aldrich
Bis(trichloromethyl) carbonate, purum, ≥99.0% (AT)