One-pot synthesis of imidazolinium salts via the ring opening of tetrahydrofuran-Reference-Cited by-同舟云学术

One-pot synthesis of imidazolinium salts via the ring opening of tetrahydrofuran

Published:2017 Issue:37 Volume:46 Page:12430-12433
ISSN:1477-9226
Container-title:Dalton Transactions
language:en
Short-container-title:Dalton Trans.

Author:

Huang Yong-Qing¹²³⁴⁵,Zhao Yue¹²³⁴⁵,Wang Peng¹²³⁴⁵,Okamura Taka-aki⁶⁷⁸⁹¹⁰^ORCID,Laforteza Brian N.¹¹¹²¹³¹⁴,Lu Yi¹²³⁴⁵,Sun Wei-Yin¹²³⁴⁵^ORCID,Yu Jin-Quan¹¹¹²¹³¹⁴

Affiliation:

1. Coordination Chemistry Institute

2. State Key Laboratory of Coordination Chemistry

3. School of Chemistry and Chemical Engineering

4. Nanjing National Laboratory of Microstructures

5. Collaborative Innovation Center of Advanced Microstructures

6. Department of Macromolecular Science

7. Graduate School of Science

8. Osaka University

9. Toyonaka, Osaka 560-0043

10. Japan

11. Department of Chemistry

12. The Scripps Research Institute

13. La Jolla

14. USA

Abstract

One-pot synthesis of C2-hydroxypropyl-substituted imidazolinium salts, active catalysts for the aza-Diels–Alder reaction, via the ring opening of THF is reported.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Inorganic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/DT/C7DT02883K

Reference43 articles.

1. One-Pot Electrosynthesis of Substituted Imidazolinium and Tetrahydropyrimidinium Salts from Secondary Alkyldiamines: An Electrochemical Route toward Ionic Liquids

2. Imidazolium and Imidazolinium Salts as Topical Antiseptics

3. Synthesis of MEN11420, a glycosylated bicyclic peptide, by intramolecular double cyclization using a chloroimidazolinium coupling reagent