881895-01-8

Upstream product

• 100-39-0 benzyl bromide 
• 881895-00-7 N-((2S,3S,4R,5S,6R)-3-Azido-5-benzyloxy-6-benzyloxymethyl-2-p-tolylsulfanyl-tetrahydro-pyran-4-yl)-acetamide 
• 881894-99-1 N-((2R,4aR,6S,7S,8R,8aS)-7-Azido-2-phenyl-6-p-tolylsulfanyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yl)-acetamide 
• 881894-97-9 (2R,4aR,6S,7S,8R,8aS)-7,8-Diazido-2-phenyl-6-p-tolylsulfanyl-hexahydro-pyrano[3,2-d][1,3]dioxine 
• 881894-96-8 p-tolyl 2-deoxy-2-azido-4,6-O-benzylidene-1-thio-β-D-altropyranoside 
• 872593-76-5 p-tolyl 2,3-anhydro-4,6-O-benzylidene-1-thio-β-D-allopyranoside 

Downstream Products

• 881895-02-9 N-{(1R,2S,3R)-1-[(S)-1-Azido-2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-2,4-bis-benzyloxy-3-hydroxy-butyl}-acetamide 
• 881894-77-5 N-[(1R,2S,3R)-1-((S)-1-Azido-2-hydroxy-ethyl)-2,3,4-tris-benzyloxy-butyl]-acetamide 
• 881895-03-0 N-{(1R,2S,3R)-1-[(S)-1-Azido-2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-2,3,4-tris-benzyloxy-butyl}-acetamide 

Relevant academic research and scientific papers

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.