93601-17-3

Upstream product

• 96287-82-0 methyl 4,6-dideoxy-2,3-O-isopropylidene-4-(methoxycarbonylamino)-3-C-methyl-α-L-mannopyranoside 
• 93474-76-1 methyl 4,6-dideoxy-3-C-methyl-4-(N-methyl-N-phenylsulfonylamino)-α-L-mannopyranoside 
• 96287-83-1 methyl 4,6-dideoxy-2,3-O-isopropylidene-3-C-methyl-4-(methylamino)-α-L-mannopyranoside 

Relevant academic research and scientific papers

SYNTHESIS OF NOVEL BRANCHED-CHAIN AMINO SUGARS: METHYL L-SIBIROSAMINIDE AND N-ACYLKANSOSAMINE

Methyl L-sibirosaminide and N-acylkansosamine were synthesized via the same intermediate, methyl 4-amino-4,6-dideoxy-2,3-O-isopropylidene-3-C-methyl-α-L-mannopyranoside (7), from L-rhamnose in 7 and 10 steps, respectively.Conversion of 7 into the title co

α-Amino Acids as Chiral Educts for Asymmetric Products. Chirospecific Syntheses of Methyl L-Sibirosaminide and Its C-3 Epimer from L-Allothreonine

Efficient syntheses of methyl L-sibirosaminide and its C-3 epimer are described using L-allothreonine as the chiral educt.Amino acylations of organometallics with the lithium salt of N-(phenylsulfonyl)-L-allothreonine constitute the key carbon-carbon bond