916599-83-2

Upstream product

• 482631-88-9 (2S,3S,4R,5R)-3,4-Bis-benzyloxy-2-iodomethyl-5-methoxy-tetrahydro-furan 
• 70831-62-8 methyl 2,3-di-O-benzyl-β-D-ribofuranoside 
• 1251531-61-9 Methyl 2,3 di-O-benzyl-5-O-trityl-D-ribofuranoside 
• 916599-82-1 (4R,5R)-4,5-Bis-benzyloxy-hept-6-en-3-one 
• 916599-91-2 (4S,5R)-4,5-Bis-benzyloxy-hept-6-en-3-ol 

Downstream Products

• 916599-94-5 (1R,2R,3R,4R,5R,6S,8R)-4,5-Bis-benzyloxy-3-(tert-butyl-dimethyl-silanyloxy)-8-(tert-butyl-dimethyl-silanyloxymethyl)-2-methyl-11-methylene-12-oxa-tricyclo[6.3.1.0^1,6]dodecane 
• 916599-85-4 acetic acid 6-[3,4-bis-benzyloxy-2-(tert-butyl-dimethyl-silanyloxy)-1-methyl-hex-5-enyl]-2-(tert-butyl-dimethyl-silanyloxymethyl)-5-oxo-5,6-dihydro-2H-pyran-2-yl ester 
• 916599-87-6 (1S,2R,3R,4R,5R,6R,8R)-4,5-Bis-benzyloxy-3-(tert-butyl-dimethyl-silanyloxy)-8-(tert-butyl-dimethyl-silanyloxymethyl)-2-methyl-12-oxa-tricyclo[6.3.1.0^1,6]dodec-9-en-11-one 
• 916599-86-5 (1R,2R,3R,4R,5R,6S,8S)-4,5-Bis-benzyloxy-3-(tert-butyl-dimethyl-silanyloxy)-8-(tert-butyl-dimethyl-silanyloxymethyl)-2-methyl-12-oxa-tricyclo[6.3.1.0^1,6]dodec-9-en-11-one 
• 916599-84-3 (1S,2S,3R,4R,5R)-4,5-Bis-benzyloxy-3-(tert-butyl-dimethyl-silanyloxy)-1-[5-(tert-butyl-dimethyl-silanyloxymethyl)-furan-2-yl]-2-methyl-hept-6-en-1-ol 
• 916600-02-7 Acetic acid (1R,2R,3R)-2,3-bis-benzyloxy-1-{(1R,2S)-2-[5-(tert-butyl-dimethyl-silanyloxymethyl)-furan-2-yl]-1-methyl-2-trimethylsilanyloxy-ethyl}-pent-4-enyl ester 
• 916600-05-0 Acetic acid (S)-6-((1R,2R,3R,4R)-2-acetoxy-3,4-bis-benzyloxy-1-methyl-hex-5-enyl)-2-(tert-butyl-dimethyl-silanyloxymethyl)-5-oxo-5,6-dihydro-2H-pyran-2-yl ester 
• 916600-04-9 Acetic acid (1R,2R,3R)-2,3-bis-benzyloxy-1-{(R)-1-[(S)-6-(tert-butyl-dimethyl-silanyloxymethyl)-6-hydroxy-3-oxo-3,6-dihydro-2H-pyran-2-yl]-ethyl}-pent-4-enyl ester 
• 916600-03-8 Acetic acid (1R,2R,3R)-2,3-bis-benzyloxy-1-{(1S,2S)-2-[5-(tert-butyl-dimethyl-silanyloxymethyl)-furan-2-yl]-2-hydroxy-1-methyl-ethyl}-pent-4-enyl ester 
• 916600-01-6 (1S,2R,3R,4S,5R)-4,5-Bis-benzyloxy-1-[5-(tert-butyl-dimethyl-silanyloxymethyl)-furan-2-yl]-2-methyl-1-trimethylsilanyloxy-hept-6-en-3-ol 

Relevant academic research and scientific papers

Studies on oxidopyrylium [5 + 2] cycloadditions: Toward a general synthetic route to the C12-hydroxy daphnetoxins

12-Hydroxydaphnetoxins, members of the structurally fascinating daphnane diterpene family, exhibit a wide range of significant biological activities. A general route to the BC-ring system of 12-hydroxy daphnetoxins is reported based on D-ribose. Depending on the choice of protecting groups and solvent, the oxidopyrylium-alkene [5 + 2] cycloaddition originating from A provides cycloadduct diastereomer B or C with good to excellent selectivity.