Functionalized imidazoliniums from the three-component domino reaction of N-formylmethylcarboxamides with amines and isocyanides-Reference-Cited by-同舟云学术

Functionalized imidazoliniums from the three-component domino reaction of N-formylmethylcarboxamides with amines and isocyanides

Published:2014 Issue:8 Volume:1 Page:909-913
ISSN:2052-4129
Container-title:Org. Chem. Front.
language:en
Short-container-title:Org. Chem. Front.

Author:

Lei Chuan-Hu¹²³⁴⁵,Zhao Liang¹²³⁴,Wang De-Xian⁵⁶⁷⁸⁹,Zhu Jieping¹⁰¹¹¹²¹³¹⁴,Wang Mei-Xiang¹²³⁴

Affiliation:

1. Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (Ministry of Education)

2. Department of Chemistry

3. Tsinghua University

4. Beijing 100084, China

5. Beijing National Laboratory for Molecular Sciences

6. CAS Key Laboratory of Molecular Recognition and Function

7. Institute of Chemistry

8. Chinese Academy of Sciences

9. Beijing 100190, China

10. Laboratory of Synthesis and Natural Products

11. Institute of Chemical Sciences and Engineering

12. Ecole Polytechnique Fédérale de Lausanne

13. EPFL-SB-ISIC-LSPN

14. 1015 Lausanne, Switzerland

Abstract

Functionalized imidazoliniums were synthesized efficiently from the three-component domino reaction of N-formylmethyl-substituted tertiary amides and enamides with amines and isocyanides.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/QO/C4QO00203B

Reference39 articles.

1. Baylis–Hillman reaction in [bdmim][PF 6 ] ionic liquid

2. An imidazolinium salt as ionic liquid for medium and strong bases

3. The preparation of new enantiopure imidazolinium salts and their evaluation as catalysts and shift reagents

4. Imidazolinium salts as catalysts for the aza-Diels–Alder reaction

5. Imidazolinium and amidinium salts as Lewis acid organocatalysts

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