162992-53-2

Upstream product

• 162895-65-0 8(R)-(Hydroxymethyl)-6(R),7(R)-dihydroxy-5(S)-3-oxa-1-azabicyclo<3.3.0>octan-2-one 
• 132295-44-4 2,5-anhydro-2,5-imino-D-glucitol 
• 881185-94-0 1-O-acetyl-3,4,6-tri-O-benzyl-2-deoxy-2-(p-toluenesulfonamido)-L-iditol 
• 881185-53-1 1-O-acetyl-3,4,6-tri-O-benzyl-2-deoxy-2-(p-toluenesulfonamido)-D-glucitol 
• 881185-90-6 Acetic acid (2S,3R,4S)-3,4-bis-benzyloxy-5-benzyloxymethyl-5-hydroxy-1-(toluene-4-sulfonyl)-pyrrolidin-2-ylmethyl ester 
• 881185-41-7 3,4,6-tri-O-benzyl-2-deoxy-2-(p-toluenesulfonamido)-D-glucitol 
• 881185-99-5 (2S,3R,4R,5R)-2-acetoxymethyl-3,4-di-O-benzyl-5-benzyloxymethyl-N-(p-toluenesulfonamido)pyrrolidine 
• 162992-52-1 8(R)-<(Benzyloxy)methyl>-6(R),7(R)-bis(benzyloxy)-5(S)-3-oxa-1-azabicyclo<3.3.0>octan-2-one 

Downstream Products

• 162895-66-1 5(R)-<(Benzyloxy)methyl>-3(R),4(R)-bis(benzyloxy)-2(S)-(hydroxymethyl)-N-methylpyrrolidine 
• 162895-79-6 N-(Benzyloxycarbonyl)-5(R)-<(benzyloxy)methyl>-3(R),4(R)-bis(benzyloxy)-2(S)-(hydroxymethyl)pyrrolidine 
• 162895-67-2 5(R)-<(Benzyloxy)methyl>-3(R),4(R)-bis(benzyloxy)-2(S)-formyl-N-methylpyrrolidine 
• 162895-80-9 N-(Benzyloxycarbonyl)-5(R)-<(benzyloxy)methyl>-3(R),4(R)-bis(benzyloxy)-2(S)-<<<(4-methylphenyl)sulfonyl>oxy>methyl>pyrrolidine 
• 162895-76-3 N-(Benzyloxycarbonyl)-5(R)-<(benzyloxy)methyl>-3(R),4(R)-bis(benzyloxy)-2(S)-<(2-amino-6-chloropurin-9-yl)methyl>pyrrolidine 
• 162895-77-4 N-(Benzyloxycarbonyl)-5(R)-<(benzyloxy)methyl>-3(R),4(R)-bis(benzyloxy)-2(S)-(9-guaninylmethyl)pyrrolidine 
• 132295-44-4 2,5-anhydro-2,5-imino-D-glucitol 

Relevant academic research and scientific papers

A glycal approach towards an efficient and stereodivergent synthesis of polyhydroxypyrrolidines

A stereo-defined synthesis of two diastereomers of polyhydroxypyrrolidines from 3,4,6-tri-O-benzyl-d-glucal 4 involving a cleavage-recyclization strategy is reported. Hemiacetal 7 obtained from glucal 4, upon reduction with LiAlH 4 afforded dio

Synthesis and evaluation of homoazasugars as glycosidase inhibitors

In an effort to develop transition-state mimetics of the glycosidase-catalyzed reaction, five- and six-membered azasugars and their homo-analogs were prepared and tested as inhibitors of glycosidases. Inhibition studies indicate that the fucosyl cationlik