Issue 3, 2016

Bargellini condensation of ninhydrin as a ketone and substituted anilines as nucleophiles

Abstract

A series of novel α-amino acids based on ninhydrin were synthesized by using various substituted anilines as nucleophiles with ninhydrin in the presence of chloroform and NaOH as base. All the compounds were fully characterized. All reactions were completed under ambient reaction conditions and all products were obtained in high to excellent yields and with high purity.

Graphical abstract: Bargellini condensation of ninhydrin as a ketone and substituted anilines as nucleophiles

Supplementary files

Article information

Article type
Letter
Submitted
05 Dec 2015
Accepted
15 Jan 2016
First published
18 Jan 2016

New J. Chem., 2016,40, 1962-1965

Bargellini condensation of ninhydrin as a ketone and substituted anilines as nucleophiles

Z. Rashid, R. Ghahremanzadeh and H. Naeimi, New J. Chem., 2016, 40, 1962 DOI: 10.1039/C5NJ03455H

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