445424-78-2

Upstream product

• 1026106-21-7 C₂₇H₃₈O₃Si 
• 445424-75-9 ethyl 6-(tert-butyldiphenylsilyloxy)-3-methylhex-2-enoate 
• 215251-69-7 4-(tert-butyldiphenylsilyloxy)-N-methoxy-N-methylbutanamide 
• 131085-31-9 5-((tert-butyldiphenylsilyl)oxy)pentan-2-one 
• 109-92-2 ethyl vinyl ether 
• 445424-76-0 6-((tert-butyldiphenylsilyl)oxy)-3-methylhex-2-en-1-ol 

Downstream Products

• 445425-11-6 (R)-4-Methyl-4-vinyl-cyclohex-2-enol 
• 445425-10-5 Trimethyl-((R)-4-methyl-4-vinyl-cyclohex-2-enyloxy)-silane 
• 445424-80-6 tert-butyl-(4-methyl-4-vinyl-hex-5-enyloxy)-diphenyl-silane 

Relevant academic research and scientific papers

Synthetic studies toward neovibsanins A and B: construction of the neovibsanin core utilizing palladium(0)-catalyzed carbonylative cyclization with carbon monoxide

The core A-ring of neovibsanins A (1) and B (2), which are potent neurotrophic agents isolated from the leaves of Viburnum awabuki, have been effectively constructed by the intramolecular palladium(0)-catalyzed carbonylative cyclization of alkenyl iodide

Diastereoselective ring-closing metathesis for the construction of a quaternary carbon stereogenic center

A diastereoselective ring-closing metathesis of the trienes 1 leading to the formation of a quaternary carbon stereogenic center on the cyclohexenes 2 has been developed.