The [2,3]-Wittig sigmatropic rearrangement of an appropriate glucose derivative followed by further chemical modification afforded stereoselectively the C-analogue of beta-D-glucopyranosyl serine.
Stereoselective synthesis of the C-analogue of beta-D-glucopyranosyl serine / L. Lay, M. Meldal, F. Nicotra, L. Panza, G. Russo. - In: CHEMICAL COMMUNICATIONS. - ISSN 1359-7345. - :15(1997), pp. 1469-1470.
Stereoselective synthesis of the C-analogue of beta-D-glucopyranosyl serine
L. LayPrimo
;
1997
Abstract
The [2,3]-Wittig sigmatropic rearrangement of an appropriate glucose derivative followed by further chemical modification afforded stereoselectively the C-analogue of beta-D-glucopyranosyl serine.
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