352312-63-1

Upstream product

• 1378314-32-9 (S)-di-tert-butyl-2-(2-methoxyphenyl)succinate 
• 1378314-69-2 C₁₁H₁₆O₃ 
• 17413-10-4 2,3-dihydro-1,4-benzodioxin-6-ylmethylamine 
• 5720-06-9 2-Methoxyphenylboronic acid 
• 865355-96-0 1-(2,3-dihydro-benzo[1,4]dioxin-6-ylmethyl)-pyrrole-2,5-dione 
• 865355-97-1 (S)-1-(2,3-Dihydro-benzo[1,4]dioxin-6-ylmethyl)-3-(2-methoxy-phenyl)-pyrrolidine-2,5-dione 

Relevant academic research and scientific papers

Preparation of chiral 3-arylpyrrolidines via the enantioselective 1,4-addition of arylboronic acids to fumaric esters catalyzed by Rh(I)/chiral diene complexes

A highly efficient rhodium-catalyzed protocol for the preparation of 2-arylsuccinic esters and 3-arylpyrrolidines of high optical purity has been achieved. In the presence of 1 mol % of a chiral diene/Rh(I) catalyst, asymmetric addition of various arylbor

Chiral phosphine-olefin bidentate ligands in asymmetric catalysis: Rhodium-catalyzed asymmetric 1,4-addition of aryl boronic acids to maleimides

(Chemical Equation Presented) Two is better than one: Novel chiral phosphine - olefin ligands 1 a and 1 b act as bidentate ligands with some transition metals and have proved to be highly effective in the rhodium-catalyzed asymmetric 1,4-addition of aryl boronic acids to maleimides with high enantio-selectivity (see scheme).