SYNTHESIS OF 1D-2-O- AND 1D-5-O-(α-D-GALACTOPYRANOSYL)-4-O-METHYL-chiro-INOSITOL: PREFERENCE FOR EQUATORIAL HYDROXYL GROUPS IN THE IMIDATE GALACTOSYLATION PROCEDURE
1D-2-O-(α-D-Galactopyranosyl)-4-O-methyl-chiro-inositol, identical to a galactosylpinitol previously isolated from seeds of Trifolium subterraneum, has been synthesized, together with an isomer, 1D-5-O-(α-D-galactopyranosyl)-4-O-methyl-chiro-inositol.In b
Garegg, Per J.,Kvarnstroem, Ingemar
p. 61 - 70
(2007/10/02)
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