Palladium-catalyzed cascade cyclization of allenamide with 2-iodoanilines to access functionalized indoloquinolines-Reference-Cited by-同舟云学术

Palladium-catalyzed cascade cyclization of allenamide with 2-iodoanilines to access functionalized indoloquinolines

Published:2023 Issue:2 Volume:21 Page:279-283
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Geng Wenzhe¹,Wang Hui¹²,Xi Juan¹,Jiang Ruonan¹,Guo Jintao¹,Jiao Keqiang¹,Tang Mengyao¹,Liu Qing¹,Zhang Lizhi¹,Liu Hui¹²^ORCID

Affiliation:

1. School of Chemistry & Chemical Engineering, Shandong University of Technology, 266 West Xincun Road, Zibo 255049, P. R. China

2. Shandong Jincheng Biopharmaceutical Co., Ltd., No. 3 Shuangshan Road of Xingshan, Zibo 255049, P. R. China

Abstract

A novel and efficient palladium-catalyzed cascade cyclization to indoloquinoline derivatives in one pot has been developed by using allenamide derivatives and 2-iodoanilines as the key building blocks.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/OB/D2OB01770A

Reference62 articles.

1. In Vitro and In Vivo Antitumor Activity of Indolo[2,3-b] Quinolines, Natural Product Analogs from Neocryptolepine Alkaloid

2. Total Synthesis of (±)-Perophoramidine

3. Total Synthesis of (+)-Perophoramidine and Determination of the Absolute Configuration

4. Construction of Vicinal All-Carbon Quaternary Stereocenters by Catalytic Asymmetric Alkylation Reaction of 3-Bromooxindoles with 3-Substituted Indoles: Total Synthesis of (+)-Perophoramidine

5. Evolution of a Unified, Stereodivergent Approach to the Synthesis of Communesin F and Perophoramidine

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