Metal-free quinolylation of the primary amino groups of amino acid derivatives and peptides with dihydrooxazolo[3,2-a]quinoliniums-Reference-Cited by-同舟云学术

Metal-free quinolylation of the primary amino groups of amino acid derivatives and peptides with dihydrooxazolo[3,2-a]quinoliniums

Published:2019 Issue:15 Volume:21 Page:4231-4237
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Liu Peng¹²³⁴⁵,Li Bo¹²³⁴⁵^ORCID,Xi Mengyu¹²³⁴⁵,Chen Zhaoqiang¹²³⁴⁵,Sun Haiguo¹²³⁴⁵,Huan Xiajuan¹²³⁴⁵,Xu Xuejun¹²³⁴⁵,Zhang Yong¹²³⁴⁵,Zou Kun¹²³⁴⁵,Jiang Xiangrui¹²³⁴⁵,Miao Zehong¹²³⁴⁵,Liu Jinggen¹²³⁴⁵,Shen Jingshan¹²³⁴⁵,Chen Kaixian¹²³⁴⁵,Zhu Weiliang¹²³⁴⁵^ORCID

Affiliation:

1. Key Laboratory of Receptor Research

2. Drug Discovery and Design Center

3. Shanghai Institute of Materia Medica

4. Chinese Academy of Sciences

5. Shanghai 201203

Abstract

A new metal-free method for theN-quinolylation of primary amino groups using novel dihydrooxazolo[3,2-a]quinoliniums showing good compatibility with other reactive moieties.

Funder

National Basic Research Program of China

National Key New Drug Creation and Manufacturing Program, Ministry of Science and Technology

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Pollution,Environmental Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/GC/C9GC01442J

Reference47 articles.

1. Peptide therapeutics: current status and future directions