Silver-catalyzed tandem cycloisomerization/hydroarylation reactions and mechanistic investigations for an efficient access to 1,2-dihydroisoquinolines-Reference-Cited by-同舟云学术

Silver-catalyzed tandem cycloisomerization/hydroarylation reactions and mechanistic investigations for an efficient access to 1,2-dihydroisoquinolines

Published:2021 Issue:5 Volume:19 Page:1037-1046
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

De Abreu Maxime¹²³⁴⁵^ORCID,Tang Yue⁶⁷⁸⁹¹⁰,Brachet Etienne¹²³⁴⁵^ORCID,Selkti Mohamed¹²³⁴⁵,Michelet Véronique⁶⁷⁸⁹¹⁰^ORCID,Belmont Philippe¹²³⁴⁵^ORCID

Affiliation:

1. Université de Paris

2. CiTCoM

3. UMR CNRS 8038

4. F-75006 Paris

5. France

6. Université Côte d'Azur

7. Institut de Chimie de Nice

8. UMR CNRS 7272

9. Parc Valrose

10. Faculté des Sciences

Abstract

A combination of AcOH and Ag catalyst induced an efficient tandem reaction to form 1,2-dihydroisoquinoline derivatives. Highly functionalized multiheterocyclic scaffolds are accessible straightforwardly using readily available starting materials.

Funder

Centre National de la Recherche Scientifique

Institut National Du Cancer

Université Côte d’Azur

Agence Nationale de la Recherche

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/OB/D0OB02197K

Reference43 articles.