New and Efficient Synthesis of 2,3,4-Trisubstituted 2H-Pyrrolo[3,4-c]quinolines via a MCR/Staudinger/Aza-Wittig Sequence-Reference-Cited by-同舟云学术

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New and Efficient Synthesis of 2,3,4-Trisubstituted 2H-Pyrrolo[3,4-c]quinolines via a MCR/Staudinger/Aza-Wittig Sequence

Published:2015-09-01 Issue:23 Volume:47 Page:3701-3710
ISSN:0039-7881
Container-title:Synthesis
language:en
Short-container-title:Synthesis

Author:

He Ping¹,Qu Feng¹,Hu Ruo-Fei¹,Gao Le¹,Wu Jing¹,Cheng Xiao-Hong²,Wang Song²

Affiliation:

1. College of Chemical Engineering and Food Science, Hubei University of Arts and Science

2. Hubei Key Laboratory of Low Dimensional Optoelectronic Materials and Devices, Hubei University of Arts and Science

Publisher

Georg Thieme Verlag KG

Subject

Organic Chemistry,Catalysis

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0035-1560208.pdf

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1. 2-Azidobenzaldehyde-Based [4+2] Annulation for the Synthesis of Quinoline Derivatives;Molecules;2024-03-11

2. Acid-Promoted Cyclization of α-Azidobenzyl Ketones through C═N Bond Formation: Synthesis of 6-Substituted Quinoline Derivatives;Organic Letters;2024-01-10

3. 2-azidobenzaldehyde: A versatile scaffold for the generation of N‐heterocyclic compounds;Journal of Molecular Structure;2023-12

4. In situ generation of imines by the Staudinger/aza-Wittig tandem reaction combined with thermally induced Wolff rearrangement for one-pot three-component β-lactam synthesis;Organic & Biomolecular Chemistry;2022

5. 1,2,3-Triazoles;Comprehensive Heterocyclic Chemistry IV;2022

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