Synthesis of 2H-pyrrolo[3,4-C]quinoline via an Aldol/Van Leusen/Staudinger/aza-Wittig sequence-Reference-Cited by-同舟云学术

Synthesis of 2H-pyrrolo[3,4-C]quinoline via an Aldol/Van Leusen/Staudinger/aza-Wittig sequence

Published:2016-08-03 Issue:16 Volume:46 Page:1357-1363
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Shi Yu-Qing¹,Liao Li-De¹,He Ping¹²,Hu Yang-Gen³,Cheng Hua¹,Wang Song²,Wu Jun-Jun¹

Affiliation:

1. College of Chemical Engineering and Food Science, Xiangyang, China

2. Hubei Key Laboratory of Low Dimensional Optoelectronic Materials and Device, Hubei University of Arts and Science, Xiangyang, China

3. Hubei Key Laboratory of Wudang Local Chinese Medicine Research and Department of Pharmacy of Taihe Hospital, Hubei University of Medicine, Shiyan, China

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/00397911.2016.1204462

Reference44 articles.

1. Aplidiopsamine A, an Antiplasmodial Alkaloid from the Temperate Australian Ascidian, Aplidiopsis confluata

2. Synthesis and cytotoxic activity of 2-dialkylamino-alkyl-1,3-dihydropyrrolo[3,4-c]quinoline-1,3-diones and 6-(2-dimethylaminoethyl)-1H-dibenz[c,e]azepine-5,7-dione

3. Synthesis and Biological Activity of 7-Phenyl-6,9-dihydro-3H-pyrrolo[3,2-f]quinolin-9-ones: A New Class of Antimitotic Agents Devoid of Aromatase Activity

4. Reversible inhibitors of the gastric (H+/K+)-ATPase. 1. 1-Aryl-4-methylpyrrolo[3,2-c]quinolines as conformationally restrained analogs of 4-(arylamino)quinolines

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