Phosphine-catalyzed [5+1] annulation of β′-acetoxy allenoates: straightforward access to tetrahydroquinoline derivatives-Reference-Cited by-同舟云学术

Phosphine-catalyzed [5+1] annulation of β′-acetoxy allenoates: straightforward access to tetrahydroquinoline derivatives

Published:2023 Issue:78 Volume:59 Page:11712-11715
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Zhu Yannan¹^ORCID,Xu Zhili¹,Wang Yi-Ning¹^ORCID

Affiliation:

1. Faculty of Chemistry and Chemical Engineering, Yancheng Institute of Technology, Yancheng 224051, China

Abstract

A phosphine-catalyzed [5+1] annulation reaction of β′-acetoxy allenoates with 1,5-dinucleophiles was developed to readily access functionalized tetrahydroquinolines in good to high yields.

Funder

Yancheng Institute of Technology

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/2023/CC/D3CC03413E

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3. Highly Potent and Selective MT2 Melatonin Receptor Full Agonists from Conformational Analysis of 1-Benzyl-2-acylaminomethyl-tetrahydroquinolines

4. Synthesis of new cis-fused tetrahydrochromeno[4,3-b]quinolines and their antiproliferative activity studies against MDA-MB-231 and MCF-7 breast cancer cell lines

5. Nonsteroidal progesterone receptor antagonists based on 6-thiophenehydroquinolines

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