1374552-65-4

Upstream product

• 1374552-70-1 (2S,3S,5R)-5-Allyl-2-[(tert-butyldimethylsilyloxy)methyl]-5-methyltetrahydrofuran-3-ol 
• 1374552-71-2 (2S,3R,5R)-5-Allyl-2-[(tert-butyldimethylsilyloxy)methyl]-5-methyltetrahydrofuran-3-ol 
• 94284-19-2 1-deoxy-2,3:4,6-di-O-isopropylidene-L-sorbofuranose 
• 17682-70-1 2,3:4,6-bis-O-isopropylidene-L-sorbose 
• 1374552-67-6 (2R,3S,4S,5S)-2-allyl-4-(benzyloxy)-5-(benzyloxymethyl)-2-methyltetrahydrofuran-3-ol 
• 1374552-68-7 1-deoxy-4-benzyloxy-5-(benzyloxymethyl)-2,3-O-isopropylidene-L-sorbofuranose 
• 1374552-77-8 C₂₂H₃₆O₃Si 
• 1374552-75-6 C₉H₁₆O₃ 
• 1374552-66-5 [(2S,3R,5R)-3-(benzyloxy)-5-methyl-5-propyltetrahydrofuran-2-yl]-methanol 
• 1374552-72-3 C₁₆H₂₂O₃ 
• 83032-06-8 (3aS,5S,6R,6aS)-5-Hydroxymethyl-2,2,3a-trimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-ol 
• 38084-00-3 1-deoxy-1-iodo-2,3:4,6-di-O-isopropylidene-α-L-sorbofuranose 

Relevant academic research and scientific papers

A carbohydrate-based synthesis of the C13-C22 fragment of amphidinolide X

A facile carbohydrate-based route was developed for the synthesis of the tetrahydrofuran (C13-C22) fragment of amphidinolide X. Starting from L-sorbose, the key reactions followed include the stereoselective synthesis of a quaternary center at C1, Barton-