2018Organic Chemistry FrontiersRequires access

Optically active N -alkyl aziridines via stereospecific reductive cyclization of α-mesylated acetamides

Duanshuai Tian, Henian Peng, Ziyue Liu, Wenjun Tang

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Abstract

An efficient method for the synthesis of optically active N -alkyl aziridines has been realized for the first time by stereospecific reductive cyclization of optically active α-mesylated acetamides. A series of optically active N -alkyl aziridines are prepared in moderate to good yields and excellent ees.

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An efficient method for the synthesis of optically active N -alkyl aziridines has been realized for the first time by stereospecific reductive cyclization of optically active α-mesylated acetamides. A series of optically active N -alkyl aziridines are prepared in moderate to good yields and excellent ees.

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Available abstract

An efficient method for the synthesis of optically active N -alkyl aziridines has been realized for the first time by stereospecific reductive cyclization of optically active α-mesylated acetamides. A series of optically active N -alkyl aziridines are prepared in moderate to good yields and excellent ees.

Key concepts: Stereospecificity, Optically active, Chemistry, Alkyl, Stereochemistry, Medicinal chemistry, Organic chemistry, Catalysis

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