Metal free direct formation of various substituted pyrido[2′,1′:2,3]imidazo[4,5-c]isoquinolin-5-amines and their further functionalization-Reference-Cited by-同舟云学术

Metal free direct formation of various substituted pyrido[2′,1′:2,3]imidazo[4,5-c]isoquinolin-5-amines and their further functionalization

Published:2015 Issue:44 Volume:5 Page:35201-35210
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Tber Z.¹²³⁴⁵,Hiebel M.-A.¹²³⁴⁵,Allouchi H.⁶⁷⁸⁹⁵,El Hakmaoui A.¹⁰¹¹¹²¹³,Akssira M.¹⁰¹¹¹²¹³,Guillaumet G.¹²³⁴⁵,Berteina-Raboin S.¹²³⁴⁵

Affiliation:

1. Institut de Chimie Organique et Analytique

2. Université d'Orléans

3. UMR CNRS 7311

4. 45067 Orléans Cédex

5. France

6. Laboratoire de Physique

7. équipe RICM UMR-ISP 1282

8. Université François Rabelais de Tours

9. Tours

10. Equipe de Chimie Bioorganique & Analytique

11. URAC 22 Université Hassan II Mohammedia-Casablanca

12. 28800 Mohammedia

13. Morocco

Abstract

Original substituted pyrido[2′,1′:2,3]imidazo[4,5-c]isoquinolin-5-amines have been easily prepared via an Groebke–Blackburn–Bienaymé MCR, then an N-deprotection followed by a spontaneous final cyclization step.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/RA/C5RA03703D

Reference39 articles.

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3. Straightforward Bienaymé and copper catalyzed N-arylation sequence to access diverse 5H-pyrido[2′,1′:2,3]imidazo[4,5-b]indoles and analogues

4. Reaction of 3-nitroso-2-phenylimidazo[1,2-a]pyridine with triethyl phosphite. A revised structure for the product

5. Synthesis and antihypertensive activity of some imidazoindole derivatives

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