M. Shimazaki

发表

Stereospecific 1,2-rearrangement of cyclopropyl group. Synthesis of chiral α-cyclopropyl ketones and α-cyclopropyl aldols

Keisuke Suzuki, M. Shimazaki, H. Hara, 1989 .

Stereoselective construction of three-and four-contiguous asymmetric centers : novel possibility by alkylative rearrangement of epoxy silyl ethers

Keisuke Suzuki, M. Shimazaki, M. Morimoto, 1990 .

Silicon-directed stereoselective synthesis of 2-vinyl-1,3-diols

Keisuke Suzuki, Mayumi Miyazawa, G. Tsuchihashi, 1988 .

On the use of epoxy alcohol-aldol rearrangement for stereoselective construction of quarternary carbon centers

Keisuke Suzuki, G. Tsuchihashi, M. Shimazaki, 1987 .

Epoxy silyl ether rearrangements: a new, stereoselective approach to the synthesis of .beta.-hydroxy carbonyl compounds

K. Maruoka, Keisuke Suzuki, M. Hasegawa, 1986 .

Stereo-divergent asymmetric total synthesis of avenaciolide and isoavenaciolide. Complete reversal of stereoselectivity in reduction of 2-vinyl aldols with / without trimethylsilyl directing group

Keisuke Suzuki, Mayumi Miyazawa, G. Tsuchihashi, 1986 .

Synthesis of 2-vinyl-1,3-diols via highly stereoselective reduction of 2-vinyl aldols using trimethylsilyl stereo-directing group

Keisuke Suzuki, G. Tsuchihashi, M. Shimazaki, 1986 .