59832-41-6

Upstream product

• 104-88-1 4-chlorobenzaldehyde 
• 120-46-7 1,3-diphenylpropanedione 

Downstream Products

• 1233126-05-0 (3-(4-chlorophenyl)-5-phenyl-2,2'-bifuran-4-yl)(phenyl)methanone 
• 1233126-08-3 (4,5-bis(4-chlorophenyl)-2-phenylfuran-3-yl)(phenyl)methanone 
• 1228602-61-6 (3R)-[3-(4-chlorophenyl)oxirane-2,2-diyl]bis(phenylmethanone) 
• 1450988-97-2 ((2'S,3'R)-1-benzyl-3'-(4-chlorophenyl)-2-oxo-5'-thioxospiro[indoline-3,2'-pyrrolidine]-4',4'-diyl)bis(phenylmethanone) 
• 1331773-67-1 4-benzoyl-3-phenyl-5-(4-chlorophenyl)-2-oxaspiro[5.5]undec-3-en-1-one 
• 1331773-62-6 9-benzoyl-8-phenyl-10-(4-chlorophenyl)-7-oxaspiro[4.5]dec-8-en-6-one 
• 1308317-29-4 [3-(4-chlorophenyl)oxirane-2,2-diyl]bis(phenylmethanone) 
• 95855-30-4 3-(4-Chlorphenyl)-4-benzoyl-N-(4-methylbenzylidene)-5-phenyl-2-furanamine 
• 95855-25-7 3-(4-Chlorphenyl)-4-benzoyl-5-hydroxy-5-phenyl-2(5H)-pyrrolone 
• 95855-20-2 2-(4-Chlorphenyl)-3-benzoyl-4-oxo-4-phenylbutanenitrile 

Relevant academic research and scientific papers

Synthesis of chiral tetrahydrofurans via catalytic asymmetric [3 + 2] cycloaddition of heterosubstituted alkenes with oxiranes

An efficient diastereo- and enantioselective [3 + 2] cycloaddition of heterosubstituted alkenes with oxiranes via selective C-C bond cleavage of epoxides has been developed. The reaction was catalyzed by a chiral N,N′-dioxide/Ni(II) catalyst, and a variety of chiral highly substituted tetrahydrofurans were obtained in up to 99% yield, 92/8 dr, and 99% ee.