512790-89-5

Upstream product

• 7540-51-4 (S)-3,7-dimethyl-6-octen-1-ol 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 387834-46-0 (R)-triethyl-(1,1,5-trimethyldec-9-ynyloxy)silane 
• 387834-44-8 (1R,5R)-(Z)-3-bromomethylene-5-(tert-butyldimethyl-silanyloxy)cyclohexanol 
• 387834-43-7 (1R,4R,6S)-(E)-2-bromomethylene-4-(tert-butyldimethylsilyloxy)-7-oxa-bicyclo[4.1.0]heptane 
• 143519-45-3 (6R)-2,6-dimethylundeca-2,10-diene 
• 10340-84-8 (S)-citronellyl bromide 
• 387834-56-2 (R)-2,6-Dimethyl-undec-10-en-2-ol 
• 387834-41-5 (3R,5R)-1-bromomethylene-3,5-bis-(tert-butyldimethylsilanyloxy)cyclohexane 
• 387834-47-1 (R)-(E)-2-[6,10-dimethyl-10-(triethylsilanyloxy)undec-1-enyl]-5,5-dimethyl[1,3,2]dioxaborolane 

Downstream Products

• 139356-40-4 (1R,3aS,7aR)-4-[2-[(3R,5R)-3,5-Bis-(tert-butyl-dimethyl-silanyloxy)-cyclohexylidene]-eth-(E)-ylidene]-1-((R)-1,5-dimethyl-5-trimethylsilanyloxy-hexyl)-7a-methyl-octahydro-indene 

Relevant academic research and scientific papers

Novel synthetic approach to 19-nor-1α,25-dihydroxyvitamin D3 and its derivatives by Suzuki-Miyaura coupling in solution and on solid support

equation presented 19-nor-1α,25-Dihydroxyvitamin D3 was synthesized by the Suzuki-Miyaura coupling of the A-ring intermediate 3, which was efficiently prepared from readily available 5-(tert-butyldimethylsilyl)oxycyclohex-2-enone (5), with the