Next Article in Journal / Special Issue
Synthesis and Biological Evaluation of New 4,5-Disubstituted-Thiazolyl Amides, Derivatives of 4-Hydroxy-Piperidine or of 4-N-Methyl Piperazine
Previous Article in Journal / Special Issue
Synthesis of 6-Nitroderivatives of Oxazolo[3,2-a]-pyridines and Their Reactions with Nucleophiles
Molecules 2003, 8(6), 467-471; doi:10.3390/80600467

Solid-Phase Synthesis of Methyl N-(pyrimidin-2-yl)glycinate

 and *
Chemistry Department, Moscow State University, Moscow 119899, Russia
* Author to whom correspondence should be addressed.
Received: 13 May 2003 / Revised: 17 June 2003 / Accepted: 17 June 2003 / Published: 30 June 2003
View Full-Text   |   Download PDF [109 KB, uploaded 18 June 2014]   |   Browse Figures


A versatile method for the preparation of N-heteroaryl substituted aminoacid derivatives is suggested. The method avoids facile diketopiperazine formation.
Keywords: Solid-phase organic synthesis; N-substituted aminoacids Solid-phase organic synthesis; N-substituted aminoacids
This is an open access article distributed under the Creative Commons Attribution License (CC BY) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Share & Cite This Article

Further Mendeley | CiteULike
Export to BibTeX |
EndNote |
MDPI and ACS Style

Ermolat'ev, D.S.; Babaev, E.V. Solid-Phase Synthesis of Methyl N-(pyrimidin-2-yl)glycinate. Molecules 2003, 8, 467-471.

View more citation formats

Related Articles

Article Metrics

For more information on the journal, click here


[Return to top]
Molecules EISSN 1420-3049 Published by MDPI AG, Basel, Switzerland RSS E-Mail Table of Contents Alert