C. Ikeura

Structure-based generation of a new class of potent Cdk4 inhibitors: new de novo design strategy and library design.

K. Fukasawa, T. Machida, Y. Iwasawa, 2001, Journal of medicinal chemistry.

Total synthesis of (-)-urdamycinone B through polyketide condensation

M. Yamaguchi, C. Ikeura, T. Minami, 1992 .

A novel approach for the development of selective Cdk4 inhibitors: library design based on locations of Cdk4 specific amino acid residues.

T Honma, K. Fukasawa, N. Kawanishi, 2001, Journal of medicinal chemistry.

A synthesis of aryl C-glycosides via polyketides

M. Yamaguchi, C. Ikeura, T. Minami, 1992 .

A New Synthesis of 1,1-Difluoro-1,3-dienes via the Coupling Reaction of 2,2-Difluorovinylboranes

C. Ikeura, T. Minami, J. Ichikawa, 1992 .

A one-pot synthesis of conjugated fluoroenynes via 2,2-difluorovinylcopper intermediates

C. Ikeura, T. Minami, J. Ichikawa, 1993 .