78788-44-0

Upstream product

• 119783-94-7 4',2''-di-O-acetyl-5-O-benzoyl-4'',6''-O-cyclohexylidene-3'-deoxy-5-epi-1,3,2',6',3''-penta-N-tosylkanamycin B 
• 933-40-4 cycloxexanone dimethyl ketal 
• 119783-92-5 3'-deoxy-1,3,2',6',3''-penta-N-tosylkanamycin B 

Downstream Products

• 119783-93-6 4',2''-di-O-acetyl-4'',6''-O-cyclohexylidene-3'-deoxy-5-epi-1,3,2',6',3''-penta-N-tosylkanamycin B 
• 119783-95-8 4',2''-di-O-acetyl-4'',6''-O-cyclohexylidene-5,3'-dideoxy-5-fluoro-1,3,2',6',3''-penta-N-tosylkanamycin B 
• 69413-95-2 5,3'-dideoxy-5-fluorokanamycin B 
• 144487-82-1 2''-O-acetyl-4'',6''-O-cyclohexylidene-3'-deoxy-1,3,2',6',3''-penta-N-tosylkanamycin B 
• 119783-93-6 4',2''-di-O-acetyl-4'',6''-O-cyclohexylidene-3'-deoxy-1,3,2',6',3''-penta-N-tosylkanamycin B 
• 144487-83-2 2''-O-acetyl-5-O-benzoyl-4'',6''-O-cyclohexylidene-3'-deoxy-5-epi-1,3,2',6',3''-penta-N-tosylkanamycin B 

Relevant academic research and scientific papers

Synthesis of 5-deoxy-5-fluoro and 5-deoxy-5,5-difluoro derivatives of kanamycin B and its analogs. Study on structure-toxicity relationships

5-Deoxy-5-fluoro- (1), 5,3'-dideoxy-5-fluoro- (2), and 5,3',4'-trideoxy-5-fluoro-kanamycin B (3) have been prepared by treatment of 5-epihydroxyl precursors (prepared by the Mitsunobu reaction) with DAST as the key step. 5,3'-Dideoxy-5,5-difluoro- (26) an