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Stereoselective Formation of Amines by Nucleophilic Addition to Azomethine Derivatives

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Stereoselective Formation of Amines

Part of the book series: Topics in Current Chemistry ((TOPCURRCHEM,volume 343))

Abstract

This chapter describes state-of-the-art methods to prepare α-chiral amines by the addition of nonstabilized nucleophiles to imine derivatives. The first part of the chapter illustrates the most effective diastereoselective addition reaction (substrate controlled and chiral auxiliary based methods) whereas the second part focuses on catalytic asymmetric methods.

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Abbreviations

DuPHOS:

[2,5-Dimethylphospholano]benzene

EWG:

Electron-withdrawing group

PG:

Protecting group

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Authors and Affiliations

  1. Faculty of Arts and Sciences, Department of Chemistry, Université de Montréal, 6128, Station Downtown, Montreal, QC, H3C 3J7, Canada

    André B. Charette & Vincent Lindsay

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  1. André B. Charette
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  2. Vincent Lindsay
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Correspondence to André B. Charette .

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Editors and Affiliations

  1. Institute of Chemical Biology and Drug Discovery, Stony Brook University, Stony Brook, New York, USA

    Wei Li

  2. Department of Chemistry & Chemical Biology, Department of Medicinal Chemistry, Rutgers, The State University of New Jersey, Piscataway, New Jersey, USA

    Xumu Zhang

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Charette, A.B., Lindsay, V. (2013). Stereoselective Formation of Amines by Nucleophilic Addition to Azomethine Derivatives. In: Li, W., Zhang, X. (eds) Stereoselective Formation of Amines. Topics in Current Chemistry, vol 343. Springer, Berlin, Heidelberg. https://doi.org/10.1007/128_2013_492

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