Intramolecular trapping of an iminium salt: rapid construction of quindoline derivatives-Reference-Cited by-同舟云学术

Intramolecular trapping of an iminium salt: rapid construction of quindoline derivatives

Published:2024 Issue:3 Volume:60 Page:292-295
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Zhou Pan¹,Wu Senhui¹,Niu Kaikai¹,Song Hongjian¹^ORCID,Liu Yuxiu¹^ORCID,Zhang Jingjing¹²,Wang Qingmin¹^ORCID

Affiliation:

1. State Key Laboratory of Elemento-Organic Chemistry, Research Institute of Elemento-Organic Chemistry, Frontiers Science Center for New Organic Matter, College of Chemistry, Nankai University, Tianjin, 300071, People's Republic of China

2. College of Basic Science, Tianjin Agricultural University, Tianjin 300384, China

Abstract

A method for synthesis of quindoline derivatives by means of intramolecular ring-closure reactions of 3-N-methylphenylindoles via an iminium salt intermediate was developed. This method can be used for the rapid synthesis of quindoline derivatives.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2024/CC/D3CC05143A

Reference51 articles.

1. Constituents of West African Medicinal Plants XX: Quindoline from Cryptolepis sanguinolenta

2. New Alkaloids from Cryptolepis sanguinolenta

3. New alkaloids from Cryptolepis sanguinolenta

4. Jusbetonin, the First Indolo[3,2-b]quinoline Alkaloid Glycoside, from Justicia betonica

5. Die Konstitution des Alkaloids Cryptolepin

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