129077-18-5

Upstream product

• 129077-17-4 methyl 2,3-di-O-benzyl-6-bromo-6-deoxy-α-D-galactopyranoside 
• 100-46-9 benzylamine 
• 7177-79-9 methyl 2,3-di-O-benzyl-4,6-O-(S)-benzylidene-α-D-galactopyranoside 
• 3396-99-4 methyl α-D-galactopyranoside 
• 64552-06-3 methyl 4,6-O-benzylidene-α-D-galactopyranoside 
• 4288-93-1 methyl 4,6-O-benzylidene-α-D-galactopyranoside 
• 29600-81-5 methyl 2,3-di-O-benzyl-4,6-O-benzylidene-α-D-galactopyranoside 
• 100-39-0 benzyl bromide 
• 29388-46-3 methyl 2,3-di-O-benzyl-α-D-galactopyranoside 

Downstream Products

• 129077-29-8 (S)-1-((2R,3S,4S)-1-Benzyl-3,4-bis-benzyloxy-pyrrolidin-2-yl)-ethane-1,2-diol 
• 129101-81-1 (S)-1-((2R,3S,4S)-1-Benzyl-3,4-bis-benzyloxy-1-oxy-pyrrolidin-2-yl)-ethane-1,2-diol 
• 129077-19-6 (2R,3S,4S)-1-Benzyl-3,4-bis-benzyloxy-2-vinyl-pyrrolidine 

Relevant academic research and scientific papers

PdCl2/CuCl2-catalysed chlorocyclisation of sugar-derived aminoalkenitols in the synthesis of new iminohexitols

The total synthesis of two novel l-ido and l-altro configured 6-chloro-1,5,6-trideoxyiminohexitols featuring a highly diastereoselective Pd(II)/CuCl2-catalysed chlorocyclisation of sugar-derived aminoalkenitols has been accomplished. The requis

A SHORT, VERSATILE APPROACH TO POLYHYDROXYLATED PYRROLIDINES UTILIZING A REDUCTIVE ELIMINATION-REDUCTIVE AMINATION AS A KEY STEP

An efficient synthesis of epimeric alpha-vinyl pyrrolidines starting from methyl 4,6-O-benzyliden gluco- and galactopyranosides gave ready access to hydroxylated pyrrolidines.