313944-65-9

Upstream product

• 313944-58-0 (1S,2R,3S,4S,5R)-3-[2-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-5-(tert-butyl-diphenyl-silanyloxymethyl)-1-methoxymethoxy-2-methyl-8-oxo-bicyclo[2.2.2]octane-2-carboxylic acid methyl ester 

Downstream Products

• 313944-66-0 (1S,2R,3S,4S,5R,8S)-3-[2-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-5-(tert-butyl-diphenyl-silanyloxymethyl)-1,8-bis-methoxymethoxy-2-methyl-bicyclo[2.2.2]octane-2-carboxylic acid methyl ester 
• 313944-67-1 [(1S,2S,3S,4S,5R,8S)-3-[2-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-5-(tert-butyl-diphenyl-silanyloxymethyl)-1,8-bis-methoxymethoxy-2-methyl-bicyclo[2.2.2]oct-2-yl]-methanol 
• 313944-62-6 ((3R,3aS,4S,6S,7S,7aS,8R)-3-Benzyloxy-4,6-bis-methoxymethoxy-3a-methyl-octahydro-4,7-ethano-inden-8-ylmethoxy)-tert-butyl-diphenyl-silane 
• 313944-68-2 2-[(1S,2S,3S,4S,6R,7S)-6-(tert-Butyl-diphenyl-silanyloxymethyl)-3-hydroxymethyl-4,7-bis-methoxymethoxy-3-methyl-bicyclo[2.2.2]oct-2-yl]-ethanol 
• 313944-60-4 (1S,2S,3aS,4S,5S,7S,7aS,9R)-9-(tert-Butyl-diphenyl-silanyloxymethyl)-5,7-bis-methoxymethoxy-7a-methyl-octahydro-4,7-ethano-indene-1,2-diol 
• 313944-70-6 (3R,3aS,4S,6S,7S,7aS,8R)-3-Benzyloxy-8-(tert-butyl-diphenyl-silanyloxymethyl)-3a-methyl-octahydro-4,7-ethano-indene-4,6-diol 
• 313944-63-7 (1R,3aS,4S,7S,7aS,9R)-1-Benzyloxy-9-(tert-butyl-diphenyl-silanyloxymethyl)-7-hydroxy-7a-methyl-octahydro-4,7-ethano-inden-5-one 
• 313944-61-5 C₃₃H₄₆O₆Si 
• 313944-69-3 (1R,3aS,4S,5S,7S,7aS,9R)-9-(tert-Butyl-diphenyl-silanyloxymethyl)-5,7-bis-methoxymethoxy-7a-methyl-octahydro-4,7-ethano-inden-1-ol 
• 313944-59-1 (1S,2R,3S,4S,5R,8S)-5-(tert-Butyl-diphenyl-silanyloxymethyl)-1,8-bis-methoxymethoxy-2-methyl-3-(2-oxo-ethyl)-bicyclo[2.2.2]octane-2-carbaldehyde 

Relevant academic research and scientific papers

Synthesis of the optically active bicyclo[4.3.0]nonane derivative, regarded as the CD ring moiety of 12-oxygenated steroids

The optically active bicyclo[4.3.0]nonane derivative, considered to be the CD ring moiety of 12-oxygenated steroids was synthesized in the present study, which involved stereo-controlled formation of bicyclo[2.2.2]octane derivative by sequential Michael reaction, formation of tricyclo[5.2.2.02,6]undecane derivative by intramolecular pinacol coupling reaction and the C-C bond cleavage by retro-aldol reaction. (C) 2000 Elsevier Science Ltd.