794517-31-0

Upstream product

• 209849-12-7 (1S)-1-((3aR,6S,6aR)-6-(benzyloxy)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl)pent-4-en-1-ol 

Downstream Products

• 1446318-78-0 5,8-anhydro-3-O-benzyl-6,7-dideoxy-1,2-O-isopropylidine-9-O-tosyl-1-glycero-β-L-ido-nonanofuranose 
• 1446318-79-1 9-C-allyl-5,8-anhydro-3-O-benzyl-6,7,9-trideoxy-1,2-O-isopropylidene-L-glycero-β-L-ido-furanose 
• 794517-26-3 Trifluoro-methanesulfonic acid (3R,4R,5R)-4,5-bis-benzyloxy-5-((2S,5R)-5-benzyloxymethyl-tetrahydro-furan-2-yl)-3-methyl-1-methylene-pentyl ester 
• 794517-41-2 (4R,5R,6R)-5,6-Bis-benzyloxy-6-((2S,5R)-5-benzyloxymethyl-tetrahydro-furan-2-yl)-4-methyl-hexan-2-ol 
• 794517-39-8 (4R,5R,6R)-5,6-Bis-benzyloxy-6-((2S,5R)-5-benzyloxymethyl-tetrahydro-furan-2-yl)-4-methyl-hexan-2-one 
• 794517-27-4 (3R,4R,5R)-4,5-Bis-benzyloxy-5-((2S,5R)-5-benzyloxymethyl-tetrahydro-furan-2-yl)-3-methyl-pentan-1-ol 
• 794517-37-6 (2R,5S)-2-Benzyloxymethyl-5-((1R,2R,3R)-1,2-bis-benzyloxy-3-methyl-pent-4-enyl)-tetrahydro-furan 
• 794517-38-7 (3R,4R,5R)-4,5-Bis-benzyloxy-5-((2S,5R)-5-benzyloxymethyl-tetrahydro-furan-2-yl)-3-methyl-pentanal 
• 794517-33-2 (2R,3R,4R,5R,2'S,5'R)-3-Benzyloxy-5'-benzyloxymethyl-5-methoxy-octahydro-[2,2']bifuranyl-4-ol 
• 794517-35-4 (2R,3R,5R,2'S,5'R)-3-Benzyloxy-5'-benzyloxymethyl-5-methoxy-4-methylene-octahydro-[2,2']bifuranyl 
• 794517-34-3 (2R,3S,5R,2'S,5'R)-3-Benzyloxy-5'-benzyloxymethyl-5-methoxy-tetrahydro-[2,2']bifuranyl-4-one 
• 794517-40-1 (1R,2R,3R)-2-Benzyloxy-1-((2S,5R)-5-benzyloxymethyl-tetrahydro-furan-2-yl)-3-methyl-pent-4-en-1-ol 
• 794517-28-5 (2R,3R,4S,5R,2'S,5'R)-3-Benzyloxy-5'-benzyloxymethyl-5-methoxy-4-methyl-octahydro-[2,2']bifuranyl 
• 794517-32-1 (3aR,5R,6S,6aR)-6-Benzyloxy-5-((2S,5R)-5-benzyloxymethyl-tetrahydro-furan-2-yl)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxole 

Relevant academic research and scientific papers

Towards the total synthesis of amphidinolide E: An enantioselective synthesis of C12-C29 fragment

An enantioselective synthesis of the C12-C29 fragment of amphidinolide E is described. Key transformations include an intramolecular mercuriocyclization reaction, stereoselective introduction of methyl group at the C2 position, and Stille coupling for the