1611459-97-2

Upstream product

• 1611459-86-9 (E)-3-[(4'R,5'R)-5'-(benzyloxy)-2',2'-dimethyl-1',3'-dioxan-4'-yl]prop-2-en-1-ol 
• 866771-99-5 [(4'R,5'R)-5'-(benzyloxy)-2',2'-dimethyl-1',3'-dioxan-4'-yl]methanol 
• 1611459-84-7 ethyl (E)-3-[(4'R,5'R)-5'-(benzyloxy)-2',2'-dimethyl-1',3'-dioxan-4'-yl]acrylate 
• 1611459-83-6 [(4'R,5'R)-5'-(benzyloxy)-2',2'-dimethyl-1',3'-dioxan-4'-yl]methyl benzoate 
• 1611459-80-3 (2R,3R)-3-(benzyloxy)-2,4-dihydroxybutyl benzoate 
• 1611459-79-0 5-O-benzoyl-3-O-benzyl-1,2-O-isopropylidene-α-D-xylofuranose 
• 34370-91-7 3-O-benzyl-1,2-O-isopropylidene-α-D-xylofuranose 
• 185541-37-1 1,2-O-isopropylidene-3-O-benzyl-5-O-triphenylmethyl-α-D-xylofuranoside 
• 1611459-96-1 C₁₈H₂₂Cl₃NO₄ 
• 1611459-95-0 C₁₈H₂₂Cl₃NO₄ 
• 1611459-87-0 (Z)-3-[(4'R,5'R)-5'-(benzyloxy)-2',2'-dimethyl-1',3'-dioxan-4'-yl]prop-2-en-1-ol 
• 866772-34-1 C₁₄H₁₈O₄ 
• 1611459-85-8 ethyl (Z)-3-[(4'R,5'R)-5'-(benzyloxy)-2',2'-dimethyl-1',3'-dioxan-4'-yl]acrylate 
• 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 
• 1611460-20-8 (4R)-3-benzyl-4-[(1'R,2'R,3'E)-1',2'-bis(benzyloxy)hexadec-3'-en-1'-yl]oxazolidin-2-one 
• 1611460-19-5 (4R)-3-benzyl-4-[(1'R,2'R,3'Z)-1',2'-bis(benzyloxy)hexadec-3'-en-1'-yl]oxazolidin-2-one 
• 1611460-21-9 C₂₇H₂₇NO₅ 
• 1611460-07-1 (4R)-4-[(4'R,5'R)-5'-(benzyloxy)-2',2'-dimethyl-1',3'-dioxan-4'-yl]oxazolidin-2-one 
• 1611460-09-3 N-{(1'R)-1'-[(4R,5R)-5-(benzyloxy)-2,2-dimethyl-1,3-dioxan-4-yl]-2'-hydroxyethyl}-2,2,2-trichloroacetamide 

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