62393-67-3

Upstream product

• 3451-36-3 (2R)-2-cyclohexylpropanoic acid 

Downstream Products

• 84850-39-5 (3S,4R)-4-Cyclohexyl-3-hydroxy-pentanoic acid tert-butyl ester 
• 84850-39-5 (3R,4R)-4-Cyclohexyl-3-hydroxy-pentanoic acid tert-butyl ester 
• 74609-13-5 (2S,4R,5S,6R)-6-Cyclohexyl-5-hydroxy-4-methyl-2-phenyl-2-trimethylsilanyloxy-heptan-3-one 
• 74609-18-0 (2S,4S,5R,6R)-6-Cyclohexyl-5-hydroxy-4-methyl-2-phenyl-2-trimethylsilanyloxy-heptan-3-one 
• 74609-14-6 (2R,4R,5S,6R)-6-Cyclohexyl-5-hydroxy-4-methyl-2-phenyl-2-trimethylsilanyloxy-heptan-3-one 
• 74609-19-1 (2R,4S,5R,6R)-6-Cyclohexyl-5-hydroxy-4-methyl-2-phenyl-2-trimethylsilanyloxy-heptan-3-one 
• 3451-36-3 (2R)-2-cyclohexylpropanoic acid 

Relevant academic research and scientific papers

Copper-Catalyzed γ-Selective and Stereospecific Allylic Cross-Coupling with Secondary Alkylboranes

The scope of the copper-catalyzed coupling reactions between organoboron compounds and allylic phosphates is expanded significantly by employing triphenylphosphine as a ligand for copper, allowing the use of secondary alkylboron compounds. The reaction proceeds with complete γ-E-selectivity and preferential 1,3-syn stereoselectivity. The reaction of γ-silicon-substituted allylic phosphates affords enantioenriched α-stereogenic allylsilanes.