Nucleophile-assisted cyclization of β-propargylamino acrylic compounds catalyzed by gold(i): a rapid construction of multisubstituted tetrahydropyridines and their fused derivatives-Reference-Cited by-同舟云学术

Nucleophile-assisted cyclization of β-propargylamino acrylic compounds catalyzed by gold(i): a rapid construction of multisubstituted tetrahydropyridines and their fused derivatives

Published:2020 Issue:21 Volume:7 Page:3356-3367
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Matouš Petr¹²³⁴⁵^ORCID,Kadaník Michal¹²³⁴⁵^ORCID,Timoracký Marek¹²³⁴⁵,Kuneš Jiří¹²³⁴⁵,Maříková Jana¹²³⁴⁵^ORCID,Růžička Aleš⁶⁷⁸⁹⁵^ORCID,Kočovský Pavel¹²³⁴⁵^ORCID,Pour Milan¹²³⁴⁵^ORCID

Affiliation:

1. Department of Organic and Bioorganic Chemistry

2. Charles University

3. Faculty of Pharmacy in Hradec Králové

4. Hradec Králové 500 05

5. Czech Republic

6. Department of General and Inorganic Chemistry

7. University of Pardubice

8. Faculty of Chemical Technology

9. 532 10 Pardubice

Abstract

A variety of medicinally important multisubstituted tetrahydropyridines, 4-aryl piperidines, isoquinolines and fused pyridines were prepared in 1–3 step sequences via nucleophile-assisted Au(i)-catalyzed cyclizations of easily available azaenynes.

Funder

Grantová Agentura České Republiky

Univerzita Karlova v Praze

European Regional Development Fund

Grantová Agentura, Univerzita Karlova

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/QO/D0QO00653J

Reference100 articles.