APA

Soloshonok V. A., Cai C., Yamada T., Ueki H., Ohfune Y. & Hruby V. J. (20060216). Michael addition reactions between chiral equivalents of a nucleophilic glycine and (S)- or (R)-3-[(E)-enoyl]-4-phenyl-1,3-oxazolidin-2-ones as a general method for efficient preparation of beta-substituted pyroglutamic acids. Case of topographically controlled stereoselectivity. : Journal of the American Chemical Society.

Chicago

Soloshonok Vadim A, Cai Chaozhong, Yamada Takeshi, Ueki Hisanori, Ohfune Yasufumi and Hruby Victor J. 20060216. Michael addition reactions between chiral equivalents of a nucleophilic glycine and (S)- or (R)-3-[(E)-enoyl]-4-phenyl-1,3-oxazolidin-2-ones as a general method for efficient preparation of beta-substituted pyroglutamic acids. Case of topographically controlled stereoselectivity. : Journal of the American Chemical Society.

Harvard

Soloshonok V. A., Cai C., Yamada T., Ueki H., Ohfune Y. and Hruby V. J. (20060216). Michael addition reactions between chiral equivalents of a nucleophilic glycine and (S)- or (R)-3-[(E)-enoyl]-4-phenyl-1,3-oxazolidin-2-ones as a general method for efficient preparation of beta-substituted pyroglutamic acids. Case of topographically controlled stereoselectivity. : Journal of the American Chemical Society.

MLA

Soloshonok Vadim A, Cai Chaozhong, Yamada Takeshi, Ueki Hisanori, Ohfune Yasufumi and Hruby Victor J. Michael addition reactions between chiral equivalents of a nucleophilic glycine and (S)- or (R)-3-[(E)-enoyl]-4-phenyl-1,3-oxazolidin-2-ones as a general method for efficient preparation of beta-substituted pyroglutamic acids. Case of topographically controlled stereoselectivity. : Journal of the American Chemical Society. 20060216.