677334-89-3

Upstream product

• 77-76-9 2,2-dimethoxy-propane 
• 677334-92-8 N-[(1S,2R,3R,4R)-2,3,5-Tris-benzyloxy-1-(1,2-dihydroxy-ethyl)-4-hydroxy-pentyl]-acetamide 
• 677334-79-1 N-(4-methoxy-benzyl)-N-[1-(1,2,4-tris-benzyloxy-3-hydroxy-butyl)-allyl]-acetamide 
• 677334-81-5 N-((3S,4R,5R,6R)-4,5,7-tris(benzyloxy)-6-hydroxyhept-1-en-3-yl)acetamide 
• 157831-25-9 (2R,3R,4R,5S)-1,3,4-Tris-benzyloxy-5-(4-methoxy-benzylamino)-hept-6-en-2-ol 
• 157831-24-8 ((3S,4R,5R)-3,4-Bis-benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-yl)-(4-methoxy-benzyl)-amine 

Downstream Products

• 677334-83-7 N-[(1S,2R,3S,4R)-2,3,5-Tris-benzyloxy-1-(2,2-dimethyl-[1,3]dioxolan-4-yl)-4-methoxymethoxy-pentyl]-acetamide 
• 677334-88-2 N-((3R,3aR,6R,6aR)-2-Benzyloxy-6-hydroxy-hexahydro-furo[3,2-b]furan-3-yl)-acetamide 
• 677334-93-9 N-((3R,3aR,6R,6aS)-2-Benzyloxy-6-methoxymethoxy-hexahydro-furo[3,2-b]furan-3-yl)-acetamide 
• 677334-87-1 O-benzyl furanodictine A 
• 677334-84-8 Toluene-4-sulfonic acid (2R,3S,4R,5R)-5-acetylamino-5-(2,2-dimethyl-[1,3]dioxolan-4-yl)-3,4-dihydroxy-2-methoxymethoxy-pentyl ester 

Relevant academic research and scientific papers

Novel and stereoselective asymmetric synthesis of an amino sugar analogue, furanodictine A

A novel and efficient strategy is described for the asymmetric synthesis of the first 3,6-anhydrosugar to be isolated from natural sources, furanodictine A. The synthetic process is based on requisite stereodefined manipulation of the functionalized amino