881894-89-9

Upstream product

• 36722-67-5 (2S,3S,4S,5S,6R)-3-Azido-4,5-bis-benzyloxy-6-benzyloxymethyl-2-methoxy-tetrahydro-pyran 
• 881894-96-8 p-tolyl 2-deoxy-2-azido-4,6-O-benzylidene-1-thio-β-D-altropyranoside 
• 943860-56-8 p-tolyl 2-deoxy-2-azido-1-thio-β-D-altropyranoside 
• 872593-76-5 p-tolyl 2,3-anhydro-4,6-O-benzylidene-1-thio-β-D-allopyranoside 
• 881895-04-1 p-tolyl 2-deoxy-2-azido-3,4,6-tri-O-benzyl-1-thio-β-D-altropyranoside 

Relevant academic research and scientific papers

An efficient synthesis of functionalized pyrrolidines and 5-epi-hyacinthacine A4 from D-glucose

The two partially protected pyrrolidines (2R,3S,AR,5R)-and (2R,3S,4R,5R)-3,4-bis(benzyloxy)-2-[(benzyloxy)methyl]-5-[(tert- butyldimethylsiloxy)methyl]pyrrolidine were synthesized from D-glucose as precursor in the stereoselective synthesis of hyacinthaci

New one-carbon degradative transformation of β-alkyl-β-azido alcohols

A new transformation of 2-azido-1-hydroxy-containing compounds to nitriles with one carbon less than the starting materials by oxidation was reported. The reaction can be performed under mild conditions.