Volume 42, Issue 1 pp. 117-120
Communication

A Diversity-Oriented Synthesis of α-Amino Acid Derivatives by a Silyltelluride-Mediated Radical Coupling Reaction of Imines and Isonitriles

Shigeru Yamago Prof.

Shigeru Yamago Prof.

Department of Synthetic Chemistry and Biological Chemistry Graduate School of Engineering, Kyoto University Kyoto 606-8501, Japan, Fax: (+81) 75-753-5911

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Hiroshi Miyazoe Dr.

Hiroshi Miyazoe Dr.

Department of Synthetic Chemistry and Biological Chemistry Graduate School of Engineering, Kyoto University Kyoto 606-8501, Japan, Fax: (+81) 75-753-5911

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Takeyoshi Nakayama

Takeyoshi Nakayama

Department of Synthetic Chemistry and Biological Chemistry Graduate School of Engineering, Kyoto University Kyoto 606-8501, Japan, Fax: (+81) 75-753-5911

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Masaki Miyoshi

Masaki Miyoshi

Department of Synthetic Chemistry and Biological Chemistry Graduate School of Engineering, Kyoto University Kyoto 606-8501, Japan, Fax: (+81) 75-753-5911

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Junichi Yoshida Prof.

Junichi Yoshida Prof.

Department of Synthetic Chemistry and Biological Chemistry Graduate School of Engineering, Kyoto University Kyoto 606-8501, Japan, Fax: (+81) 75-753-5911

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First published: 14 January 2003
Citations: 36

This work was partly supported by a Grant-in-Aid for the Scientific Research from Japan Society for the Promotion of Science.

Graphical Abstract

A radical idea: A diversity-oriented synthesis of α-amino acid derivatives is realized by the silyltelluride-mediated radical coupling of imines and isonitriles followed by various transformations of the carbon–tellurium bond of the coupling products (see scheme). The α-amino radical generated from the imine and the silyltelluride is the key intermediate in the coupling reaction.

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