53269-95-7

Upstream product

• 4291-69-4 2,3,4,6-Tetra-O-benzyl-D-glucopyranose 
• 100-53-8 phenylmethanethiol 
• 143888-85-1 (2-bromophenyl)methanethiol 
• 6919-96-6 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide 

Downstream Products

• 437757-90-9 benzyl S,S-dioxo-2,3,4,6-tetra-O-benzyl-1-thio-β-D-glucopyranoside 
• 105539-37-5 (E)-2,6-anhydro-3,4,5,7-tetra-O-benzyl-1-deoxy-1-phenyl-D-gluco-hept-1-enitol 
• 216869-51-1 (1(1')-Z)-2,3,4,6-tetra-O-benzyl-1-deoxy-1-(phenyl)methylidene-D-glucopyranose 
• 437758-24-2 (R)-phenylbromomethyl S,S-dioxo-2,3,4,6-tetra-O-benzyl-1-thio-β-D-glucopyranoside 
• 437758-25-3 (S)-phenylbromomethyl S,S-dioxo-2,3,4,6-tetra-O-benzyl-1-thio-β-D-glucopyranoside 

Relevant academic research and scientific papers

1,2-trans-1-Dihydroxyboryl benzyl S-glycoside as glycosyl donor

Activated by NBS, readily available 1,2-trans-1-dihydroxyboryl benzyl S-glycosides served as glycosyl donors and reacted with certain simple alcohol acceptors to produce pure 1,2-cis-O-glycosides in moderate yields. The boronic acid moiety was revealed es

A new route to exo-glycals using the Ramberg-Baecklund rearrangement

A new route to exo-glycals 4 is described in which glycosyl sulfones 3 are subjected to the Meyers variant of the Ramberg-Baecklund rearrangement. The conversion of sulfones derived from glucose, galactose, mannose, cellobiose, and ribose into di-, tri-, and tetra-substituted alkenes is reported. Preliminary mechanistic studies of this process are also described. Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002.