K. Yabu

Switching enantiofacial selectivities using one chiral source: catalytic enantioselective synthesis of the key intermediate for (20S)-camptothecin family by (S)-selective cyanosilylation of ketones.

M. Kanai, Y. Hamashima, M. Shibasaki, 2001, Journal of the American Chemical Society.

New entries in Lewis acid-Lewis base bifunctional asymmetric catalyst: catalytic enantioselective Reissert reaction of pyridine derivatives.

Masato Suzuki, M. Kanai, M. Shibasaki, 2004, Journal of the American Chemical Society.

Catalytic enantioselective synthesis of (20s)-camptothecin intermediates using cyanosilylation of ketones promoted by D-glucose-derived lanthanide catalyst

M. Kanai, M. Shibasaki, D. Curran, 2003 .

Total Synthesis of (−)-Verrucarol1

K. Tadano, R. Shiraki, J. Ishihara, 1998 .

Practical synthesis of chiral ligands for catalytic enantioselective cyanosilylation of ketones

M. Kanai, M. Shibasaki, S. Masumoto, 2002 .

Efficient Synthesis of a Key Intermediate of Neurokinin Receptor Antagonists Using a Bifunctional Asymmetric Catalyst

M. Kanai, M. Shibasaki, T. Nishi, 2003 .

Studies toward practical synthesis of (20S)-camptothecin family through catalytic enantioselective cyanosilylation of ketones: improved catalyst efficiency by ligand-tuning

M. Kanai, M. Shibasaki, D. Curran, 2002 .

A Platform for the Discovery of New Macrolide Antibiotics

Andrew G. Myers, Peter M. Wright, Xiang Zhou, 2016, Nature.