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Beilstein-Institut, Beilstein Journal of Organic Chemistry, (15), p. 1722-1757, 2019

DOI: 10.3762/bjoc.15.168

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N-(1-Phenylethyl)aziridine-2-carboxylate esters in the synthesis of biologically relevant compounds

This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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Abstract

Since Garner’s aldehyde has several drawbacks, first of all is prone to racemization, alternative three-carbon chirons would be of great value in enantioselective syntheses of natural compounds and/or drugs. This review article summarizes applications of N-(1-phenylethyl)aziridine-2-carboxylates, -carbaldehydes and -methanols in syntheses of approved drugs and potential medications as well as of natural products mostly alkaloids but also sphingoids and ceramides and their 1- and 3-deoxy analogues and several hydroxy amino acids and their precursors. Designed strategies provided new procedures to several drugs and alternative approaches to natural products and proved efficiency of a 2-substituted N-(1-phenylethyl)aziridine framework as chiron bearing a chiral auxiliary.