Function of an N-heterocyclic carbene ligand based on concept of chiral mimetic

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Abstract

Function of a new N-heterocyclic carbene ligand based on the concept of a chiral mimetic is described. With (4R,5R)-4,5-diphenyl-1,3-dialkyl-4,5-dihydro- 3H-imidazol-1-ium tetrafluoroborates as N-heterocyclic carbene precursors, Rh-catalyzed enantioselective arylation (up to 27% ee) of aromatic aldehydes with arylboronic acids and Pd-catalyzed enantioselective intramolecular α-arylation (up to 66% ee) of N-(2-bromoaryl)-N-alkyl-2-arylpropanamides are investigated. © 2006 Pharmaceutical Society of Japan.

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APA

Arao, T., Sato, K., Kondo, K., & Aoyama, T. (2006). Function of an N-heterocyclic carbene ligand based on concept of chiral mimetic. Chemical and Pharmaceutical Bulletin, 54(11), 1576–1581. https://doi.org/10.1248/cpb.54.1576

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