129443-62-5

Upstream product

• 14131-84-1 2,3:5,6-di-O-isopropylidene-α-D-mannofuranose 
• 129354-25-2 [2-Amino-1-((3aR,4S,6S,6aS)-6-methoxy-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-ethyl]-methyl-phosphinic acid methyl ester; hydrochloride 
• 27954-10-5 methyl 2,3-O-isopropylidene-α-D-mannofuranoside 
• 33985-40-9 1-O-methyl-2,3-O-isopropylidene-α-D-mannopentoaldo-1,4-furanose 
• 125426-08-6 Methyl (5R and 5S)-5,6-Dideoxy-2,3-O-isopropylidene-5-<(R and S)-(methoxy)methylphosphinyl>-6-nitro-α-D-lyxo-hexofuranosides 
• 125474-07-9 Methyl 5,6-Dideoxy-2,3-O-isopropylidene-6-nitro-α-D-lyxo-hex-5-enofuranoside 
• 125426-10-0 Methyl (5R and 5S)-5-Deoxy-2,3-O-isopropylidene-5-<(R and S)-(methoxy)methylphosphinyl>-α-lyxo-hexofuranosides 
• 76-83-5 trityl chloride 
• 85339-08-8 6-Deoxy-2,3-O-isopropylidene-6-nitro-α-D-lyxo-hexofuranoside 

Relevant academic research and scientific papers

Synthesis of 5-Deoxy-5--α,β-D-mannopyranoses. The First P-in-Ring Sugar Analogues of D-mannose Type

Starting with methyl 2,3-O-isopropylidene-α-D-lyxo-pentodialdo-1,4-furanoside, methyl 5-deoxy-2,3-O-isopropylidene-5--α-D-lyxo-hexofuranoside (8) was prepared (in 5 steps, 16percent overall yield).The hexose 8 was converted into