Dehydrogenative cyclization of N-acyl dipeptide esters for the synthesis of imidazolidin-4-ones-Reference-Cited by-同舟云学术

Dehydrogenative cyclization of N-acyl dipeptide esters for the synthesis of imidazolidin-4-ones

Published:2015 Issue:13 Volume:5 Page:9815-9818
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Yu Hui¹²³⁴,Shen Jie¹²³⁴

Affiliation:

1. Department of Chemistry

2. Tongji University

3. Shanghai

4. P. R. China

Abstract

Dehydrogenative cyclization of N-acyl dipeptide esters was developed and imidazolidin-4-ones were obtained in moderate to good yields by using TBHP as oxidant and KI as catalyst under mild conditions.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/RA/C4RA15019H

Reference37 articles.

1. Sequential and Spatial Organization of Metal Complexes Inside a Peptide Duplex

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4. The 2013 SFRBM discovery award: Selected discoveries from the butterfield laboratory of oxidative stress and its sequela in brain in cognitive disorders exemplified by Alzheimer disease and chemotherapy induced cognitive impairment

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