75400-53-2

Upstream product

• 1073-67-2 4-vinylbenzyl chloride 
• 21205-91-4 9-borabicyclo[3.3.1]nonane dimer 

Downstream Products

• 1261270-13-6 5-(4-chlorophenyl)-3-methyl-1-(1-methyl-1H-imidazol-2-yl)-1-pentanone 
• 1387007-48-8 (R)-5-(4-chlorophenyl)-1-(1-methyl-1H-benzimidazol-2-yl)-3-phenyl-1-pentanone 
• 5739-39-9 3-(4-chlorophenyl)-1-phenylpropan-1-one 
• 1378249-80-9 (E)-benzyl[1-(4-chlorophenyl)-4-hexen-3-yl]dimethylsilane 
• 1378249-79-6 (E)-benzyl[1-(4-chlorophenyl)-4-hexen-3-yl]dimethylsilane 
• 1378249-75-2 (E)-[1-(4-chlorophenyl)-4-hexen-3-yl]dimethylphenylsilane 
• 1378249-76-3 (E)-[1-(4-chlorophenyl)-4-hexen-3-yl]dimethylphenylsilane 

Relevant academic research and scientific papers

Palladium-Catalyzed Carbonylative Cross-Coupling of Difluoroalkyl Halides with Alkylboranes under 1 atm of CO

A palladium catalyzed carbonylative cross-coupling of difluoroalkyl halides with alkyl-9-BBN under 1 atm of CO has been developed. The reaction shows broad substrate scope and high functional group tolerance, even toward complex pharmaceuticals, providing

Enantioselective conjugate addition of alkylboranes catalyzed by a copper- N-heterocyclic carbene complex

The first catalytic enantioselective conjugate addition of alkylboron compounds has been achieved. Reactions between alkylboranes and imidazol-2-yl α,β-unsaturated ketones proceeded with high enantioselectivity under the influence of a Cu(I) catalyst syst