88199-72-8

Upstream product

• 10284-63-6 pinitol 
• 3150-24-1 4-nitrophenyl-β-D-galactopyranoside 
• 78077-14-2 1D-1,5-di-O-benzoyl-3-O-benzyl-4-O-methyl-chiro-inositol 
• 78077-18-6 1D-3-O-benzyl-4-O-methyl-2-O-(2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl)-chiro-inositol 
• 70267-71-9 2,3,4,6-tetra-O-benzyl-1-O-(N-methylacetimidoyl)-β-D-galactopyranose 

Relevant academic research and scientific papers

Enzyme-catalysed synthesis of galactosylated 1D- and 1L-chiro-inositol, 1D-pinitol, myo-inositol and selected derivatives using the β-galactosidase from the thermophile Thermoanaerobacter sp. strain TP6-B1

The products from the enzymatic β-D-galactopyranosylation of 1D-chiro-inositol, 1D-pinitol, 1D-3-O-allyl-4-O-methyl-chiro-inositol, 1D-3,4-di-O-methyl-chiro-inositol, 1L-chiro-inositol and myo-inositol in combined yields ranging from 46% to 64% have been

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