888410-75-1

Upstream product

• 38651-65-9 (1R,5S)-(+)-nopinone 

Downstream Products

• 1027754-43-3 C₂₄H₃₃N₃ 
• 1027754-40-0 C₂₁H₂₇N₃ 
• 1431378-05-0 (7R,9R)-8,8-dimethyl-2-phenyl-6,7,8,9-tetrahydro-7,9-methanoimidazo[1,5-a]quinolin-2-ium chloride 
• 1431378-06-1 (7R,9R)-2-mesityl-8,8-dimethyl-6,7,8,9-tetrahydro-7,9-methanoimidazo[1,5-a]quinolin-2-ium chloride 
• 1431378-07-2 (7R,9R)-2-(2,6-diisopropylphenyl)-8,8-dimethyl-6,7,8,9-tetrahydro-7,9-methanoimidazo[1,5-a]quinolin-2-ium chloride 
• 1431378-08-3 (7R,9R)-2-(4-methoxyphenyl)-8,8-dimethyl-6,7,8,9-tetrahydro-7,9-methanoimidazo[1,5-a]quinolin-2-ium chloride 
• 1431378-09-4 (7R,9R)-2-(3,5-bis(trifluoromethyl)phenyl)-8,8-dimethyl-6,7,8,9-tetrahydro-7,9-methanoimidazo[1,5-a]quinolin-2-ium chloride 

Relevant academic research and scientific papers

Chiral imidazo[1,5-a]tetrahydroquinoline N-heterocyclic carbenes and their copper complexes for asymmetric catalysis

Abstract Novel chiral imidazo[1,5-a]tetrahydroquinoline N-heterocyclic carbenes derived from β-pinene have been developed. The preliminary studies with both the in situ generated and preformed copper-carbene complexes have shown these chiral NHCs are efficient and selective ligands in the Cu-catalyzed asymmetric conjugate borylation of α,β-unsaturated esters.