864444-89-3

Upstream product

• 864444-87-1 (3aR,4R,6S,7S,7aS)-6-[(S)-2-(tert-Butyl-dimethyl-silanyloxy)-1-hydroxy-1-phenyl-ethyl]-2,2,4-trimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-7-ol 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 51246-20-9 1-phenyl-1-iodoethylene 
• 864444-86-0 2-(tert-butyl-dimethyl-silanyloxy)-1-phenyl-1-(2,2,4-trimethyl-3a,7a-dihydro-4H-[1,3]dioxolo[4,5-c]pyran-6-yl)-ethanol 
• 864444-84-8 (S)-1-Phenyl-1-((3aR,4R,7aS)-2,2,4-trimethyl-3a,7a-dihydro-4H-[1,3]dioxolo[4,5-c]pyran-6-yl)-ethane-1,2-diol 
• 864444-82-6 2,2,4-trimethyl-6-(1-phenyl-vinyl)-3a,7a-dihydro-4H-[1,3]dioxolo[4,5-c]pyran 

Downstream Products

• 623148-33-4 (2R)-methyl 3,7-anhydro-2-phenyl-5-O-methyl-8-deoxy-α-D-altro-octitolate 
• 864444-95-1 (R)-[(3aR,4R,6S,7S,7aR)-7-(tert-Butyl-dimethyl-silanyloxy)-2,2,4-trimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-6-yl]-hydroxy-phenyl-acetic acid methyl ester 
• 864444-99-5 (R)-[(2S,3S,4R,5S,6R)-3-(tert-Butyl-dimethyl-silanyloxy)-4,5-dihydroxy-6-methyl-tetrahydro-pyran-2-yl]-hydroxy-phenyl-acetic acid methyl ester 
• 864444-94-0 (R)-[(3aR,4R,6S,7S,7aR)-7-(tert-Butyl-dimethyl-silanyloxy)-2,2,4-trimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-6-yl]-hydroxy-phenyl-acetaldehyde 
• 864445-02-3 (3R,3aS,5R,6R,7R,7aS)-3,6-Dihydroxy-7-methoxy-5-methyl-3-phenyl-hexahydro-furo[3,2-b]pyran-2-one 
• 864445-00-1 (3R,3aS,5R,6S,7R,7aS)-3,6,7-Trihydroxy-5-methyl-3-phenyl-hexahydro-furo[3,2-b]pyran-2-one 
• 864444-91-7 (S)-1-[(3aR,4R,6S,7S,7aR)-7-(tert-Butyl-dimethyl-silanyloxy)-2,2,4-trimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-6-yl]-1-phenyl-ethane-1,2-diol 

Relevant academic research and scientific papers

Synthesis of the branched C-glycoside substructure of altromycin B

(Chemical Equation Presented) Tungsten-catalyzed cycloisomerization of alkynyl alcohols including 8 provides only the endocyclic enol ether (11) as a key intermediate for the branched Oglycoside substructure (2) of altromycin B. A sequence of Stille cross