Optically active N -alkyl aziridines via stereospecific reductive cyclization of α-mesylated acetamides
Duanshuai Tian, Henian Peng, Ziyue Liu, Wenjun Tang
Abstract
Duanshuai Tian, Henian Peng, Ziyue Liu, Wenjun Tang
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.
OpenAlex reports 4 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
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