593280-25-2

Upstream product

• 131529-43-6 methyl 3-O-benzyl-4,6-O-benzylidene-2-deoxy-2-C-(prop-2-enyl)-α-D-altropyranoside 
• 3169-98-0 methyl 4,6-O-benzylidene-2,3-dideoxy-α-D-erythro-hex-2-enopyranoside 

Downstream Products

• 799804-64-1 1-(methyl 3-O-benzyl-4,6-O-benzylidene-2-deoxy-α-D-altropyranosid-2-yl)4-phenylbut-3-yn-2-ol 
• 593280-27-4 2-amino-5-(methyl 3-O-benzyl-4,6-O-benzylidene-2-deoxy-α-D-altropyranosid-2-yl)thiophene-3-carbonitrile 
• 799804-65-2 1-(methyl 3-O-benzyl-4,6-O-benzylidene-2-deoxy-α-D-altropyranosid-2-yl)-4-phenyl-but-3-yn-2-one 
• 594837-79-3 2-cyano-4-(methyl 3-O-benzyl-4,6-O-benzylidene-2-deoxy-α-D-altropyranosid-2-yl)crotononitrile 

Relevant academic research and scientific papers

Synthesis of C-nucleoside analogues starting from 1-(methyl 3-O-benzyl-4,6-O-benzylidene-2-deoxy-α-D-altropyranosid-2-yl) -4-phenyl-but-3-yn-2-one

1-(Methyl 3-O-benzyl-4,6-O-benzylidene-2-deoxy-α-D-altropyranosid-2- yl)-4-phenyl-but-3-yn-2-one (4) was synthesized by the reaction of (methyl 3-O-benzyl-4,6-O-benzylidene-2-deoxy-α-D-altropyranosid-2-yl)ethanal (2) with lithium phenylethynide and follow

Synthesis of (methyl 3-O-benzyl-4,6-O-benzylidene-2-deoxy-α-D-altropyranosid-2-yl)thiophene derivatives as precursors of new iso-C-nucleoside analogues

Treatment of 2-(methyl 3-O-benzyl-4,6-O-benzylidene-2-deoxy-α-D-altropyranosid-2-yl)ethanal (3) with malononitrile in the presence of aluminium oxide provided 2-cyano-4-(methyl 3-O-benzyl-4,6-O-benzylidene-2-deoxy-α-D-altropyranosid-2-yl) crotononitrile (