29741-76-2

Upstream product

• 29881-47-8 1L-(1,3/2,4,6)-4,6-di-(ethoxycarbonylamido)-1,2-O-isopropylidene-1,2,3-cyclohexanetriol 
• 14429-30-2 2-Desoxystreptamin-dihydrochlorid 
• 1609-47-8 diethyl dicarbonate 
• 29741-74-0 1,6:3,4-Di-N,O-carbonyl-2-desoxystreptamin 
• 141-52-6 sodium ethanolate 
• 137555-75-0 (3aR,4S,5R,7S,7aR)-7-Amino-2,2-dimethyl-5-nitro-hexahydro-benzo[1,3]dioxol-4-ol 
• 2037-48-1 2-deoxystreptamine 
• 33639-83-7 N,N'-bis-phenoxycarbonyl-2-deoxy-streptamine 

Downstream Products

• 51995-25-6 4,5,6-Tri-O-acetyl-1,3-bis-N-(ethoxycarbonyl)-2-desoxystreptamin 
• 74342-44-2 1,3-Di-N-benzyl-5,6-di-O-benzyl-3,4-N,O-carbonyl-1-N-ethoxycarbonyl-2-desoxystreptamin 
• 74342-43-1 Pentabenzyl-1,3-di-N-ethoxycarbonyl-2-desoxystreptamin 

Relevant academic research and scientific papers

Cyclitol Reactions, I. Syntheses of New Aminocyclitols by Conversion of 2-Desoxystreptamine Derivatives

Starting from 2-deoxystreptamine several derivatives were synthesized which are selectively blocked by mesyl-, tosyl-, benzyl-, and N,O-carbonyl groups.From 1,3-N,N-carbonyl-4-O-mesyl-2-deoxystreptamine (25) the epoxide 24 was made accessible which can re