Abstract

Tailor-made amino acids are indispensable structural components of modern medicinal chemistry and drug design. Consequently, stereo-controlled preparation of amino acids is the area of high research activity. Over last decade, application of Ni(II) complexes of Schiff bases derived from glycine and chiral tridentate ligands has emerged as a leading methodology for the synthesis of various structural types of amino acids. This review article summarizes examples of asymmetric synthesis of tailor-made α-amino acids via the corresponding Ni(II) complexes, reported in the literature over the last four years. A general overview of this methodology is provided, with the emphasis given to practicality, scalability, cost-structure and recyclability of the chiral tridentate ligands.

Highlights

  • Tailor-made amino acids (AAs) [1] are essential structural features of modern medicinal chemistry and drug design

  • We summarize examples of asymmetric synthesis of tailor-made α-AAs via via the the corresponding complexes, reported in over last years

  • Complexes as the methodology of choice for asymmetric syntheses of tailor-made AA

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Summary

Introduction

Tailor-made amino acids (AAs) [1] are essential structural features of modern medicinal chemistry and drug design. The presence of orthogonal amino and carboxyl groups in adaptable proximity (α-, β-, γ-, etc.), combined with elements of chirality and diverse side chains, provides an exceptional three-dimensional structural framework with a high degree of chemical/biological functionality. These properties make AAs ideally suited for syntheses of complex molecules, highly diverse elements for SAR campaigns, basic components of modern pharmaceuticals [2,3,4,5]. Transformations of chiral Ni(II) complexes of Schiff bases derived from tridentate ligands and Molecules 2020, 25, 2739; doi:10.3390/molecules25122739 www.mdpi.com/journal/molecules

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