1611459-84-7

Upstream product

• 34370-91-7 3-O-benzyl-1,2-O-isopropylidene-α-D-xylofuranose 
• 1611459-79-0 5-O-benzoyl-3-O-benzyl-1,2-O-isopropylidene-α-D-xylofuranose 
• 866771-99-5 [(4'R,5'R)-5'-(benzyloxy)-2',2'-dimethyl-1',3'-dioxan-4'-yl]methanol 
• 1611459-83-6 [(4'R,5'R)-5'-(benzyloxy)-2',2'-dimethyl-1',3'-dioxan-4'-yl]methyl benzoate 
• 185541-37-1 1,2-O-isopropylidene-3-O-benzyl-5-O-triphenylmethyl-α-D-xylofuranoside 
• 867-13-0 diethoxyphosphoryl-acetic acid ethyl ester 
• 866772-34-1 C₁₄H₁₈O₄ 
• 1099-45-2 ethyl (triphenylphosphoranylidene)acetate 
• 1611459-82-5 C₁₈H₁₈O₅ 

Downstream Products

• 1611460-11-7 (4R)-4-[(1'R,2'R)-2'-(benzyloxy)-1',3'-dihydroxypropyl]oxazolidin-2-one 
• 1611460-13-9 (4R)-4-[(1'R,2'R)-2'-(benzyloxy)-1'-hydroxy-3'-(trityloxy)propyl]oxazolidin-2-one 
• 1611460-15-1 (4R)-3-benzyl-4-[(1'R,2'R)-1',2'-bis(benzyloxy)-3'-(trityloxy)propyl]oxazolidin-2-one 
• 1611460-17-3 (4R)-3-benzyl-4-[(1'R,2'R)-1',2'-bis(benzyloxy)-3'-hydroxypropyl]oxazolidin-2-one 
• 1611460-18-4 (4S)-3-benzyl-4-[(1'R,2'R)-1',2'-bis(benzyloxy)-3'-hydroxypropyl]oxazolidin-2-one 
• 1611460-23-1 (4S)-3-benzyl-4-[(1'R,2'R,3'E)-1',2'-bis(benzyloxy)hexadec-3'-en-1'-yl]oxazolidin-2-one 
• 1611460-22-0 (4S)-3-benzyl-4-[(1'R,2'R,3'Z)-1',2'-bis(benzyloxy)hexadec-3'-en-1'-yl]oxazolidin-2-one 
• 1611459-89-2 C₁₇H₂₄O₆S 
• 1611459-95-0 C₁₈H₂₂Cl₃NO₄ 
• 1611459-97-2 N-{(1'R)-1-[(4''R,5''R)-5''-(benzyloxy)-2'',2''-dimethyl-1'',3''-dioxan-4''-yl]allyl}-2,2,2-trichloroacetamide 
• 1611459-99-4 N-{(1'S)-1-[(4''R,5''R)-5''-(benzyloxy)-2'',2''-dimethyl-1'',3''-dioxan-4''-yl]allyl}-2,2,2-trichloroacetamide 
• 1611460-00-4 C₁₈H₂₅NO₄S 
• 1611460-04-8 C₁₈H₂₅NO₄S 
• 1611460-06-0 methyl {(1S)-1-[(4'R,5'R)-5'-(benzyloxy)-2',2'-dimethyl-1',3'-dioxan-4'-yl]-2-hydroxyethyl}carbamate 

Relevant academic research and scientific papers

Total synthesis of (-)-jaspine B and its 4-epi-analogue from d-xylose

The total synthesis of the HCl salts of (-)-jaspine B ent-1 and its 4-epi-congener ent-4 was accomplished starting from the common template 13 derived from d-xylose. The cornerstone of our synthesis was [3,3]- heterosigmatropic rearrangements, which effec