182124-65-8

Upstream product

• 182124-66-9 (2S,3S,4S,5R,6R)-1,3,4,5-Tetrakis-benzyloxy-7-(tert-butyl-dimethyl-silanyloxy)-heptane-2,6-diol 
• 79258-18-7 (2R,3R,4R,5S)-1,3,4,5-tetrakis(benzyloxy)hept-6-en-2-ol 

Downstream Products

• 1262890-07-2 3,4,5,7-tetra-O-benzyl-1,2-O-benzylidene-D-glycero-D-gulitol 
• 1262890-11-8 methyl-2,3,4,5,7-penta-O-benzyl-D-glycero-D-gulo-septanoside 
• 1262890-12-9 allyl-2,3,4,5,7-penta-O-benzyl-D-glycero-D-gulo-septanoside 
• 1262890-08-3 2,3,4,5,7-penta-O-benzyl-D-glycero-D-gulitol 
• 1262890-09-4 2,3,4,5,7-penta-O-benzyl-1,6-bis-O-triethylsilyl-D-glycero-D-gulitol 
• 1262890-10-7 2,3,4,5,7-penta-O-benzyl-6-O-triethylsilyl-D-glycero-D-gulose 

Relevant academic research and scientific papers

Tandem cyclization and acetalization of a homologated D-glucose delivers D-glycero-D-gulo-septanosides

A synthesis of methyl-D-glycero-D-gulo-septanoside and allyl D-glycero-D-gulo-septanoside from a D-glucose derived heptenitol is reported. Key steps in the synthesis include the diasteroselective dihydroxylation of the heptenitol, regioselective opening o

Chemical synthesis of β-homonojirimycin, of its N-butyl derivative, and of 'methyl homoazacellobioside'

β-Homonojirimycin (2) was prepared by the highly stereoselective double reductive amination of a 2,6-heptodiulose derivative (6 or 13) using ammonium formate and NaBH3CN. The process was unsuccessful with primary amines. The synthesis of N-buty