561018-06-2

Upstream product

• 6974-32-9 1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose 
• 115141-23-6 1-deoxy-1-diethylmethylsilyloxymethyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose 
• 561017-94-5 (2S,3R,4S,5R)-2-(tert-Butyl-diphenyl-silanyloxymethyl)-5-hydroxymethyl-tetrahydro-furan-3,4-diol 
• 561017-96-7 2,5-anhydro-1-O-tert-butyldiphenylsilyl-3,4-O-isopropylidene-D-allitol 
• 561017-98-9 2,5-anhydro-1-O-tert-butyldiphenylsilyl-3,4-O-isopropylidene-5-C-hydroxymethyl-D-allitol 
• 561017-53-6 1-deoxy-1-hydroxymethyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose 
• 561017-92-3 2,5-anhydro-3,4,6-tri-O-benzoyl-1-O-butyldiphenylsilyl-D-allitol 
• 561018-00-6 2,5-anhydro-1-O-tert-butyldiphenylsilyl-3,4-O-isopropylidene-5-C-mesyloxymethyl-6-O-mesyl-D-allitol 
• 561018-02-8 2,5-anhydro-1-O-tert-butyldiphenylsilyl-5-C-mesyloxymethyl-6-O-mesyl-D-allitol 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 561018-04-0 2,5-anhydro-1-O-tert-butyldiphenylsilyl-6-O-mesyl-4-O,5-C-methylene-D-allitol 

Downstream Products

• 561018-08-4 2,5-anhydro-6-tert-butoxycarbonylamino-1-O-tert-butyldiphenylsilyl-6-deoxy-4-O,5-C-methylene-D-allitol 

Relevant academic research and scientific papers

Synthesis of bridged sugar amino acids: A new entry into conformationally locked δ- and ε-amino acids

The synthesis of three methylene bridged sugar amino acids is described. Key transformations in the synthetic strategy are a CO-insertion on fully protected ribose, an aldol condensation with formaldehyde and an oxetane forming cyclisation step. A novel L