Sodium sulfide-promoted regiodefined redox condensation of <i>o</i>-nitroanilines with aryl ketones to benzo[<i>a</i>]phenazines and quinoxalines-Reference-Cited by-同舟云学术

Sodium sulfide-promoted regiodefined redox condensation of o-nitroanilines with aryl ketones to benzo[a]phenazines and quinoxalines

Published:2024 Issue: Volume: Page:
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Le Duc Long¹²,Nguyen Le Anh¹²,Vo Ngoc Binh¹²,Nguyen Thi Thu Tram³,Ngo Quoc Anh¹,Retailleau Pascal⁴,Nguyen Thanh Binh⁴^ORCID

Affiliation:

1. Institute of Chemistry, Vietnam Academy of Science and Technology, 18 Hoang Quoc Viet, Cau Giay, Hanoi, Vietnam

2. Graduate University of Science and Technology, Vietnam Academy of Science and Technology, 18 Hoang Quoc Viet, Cau Giay, Hanoi, Vietnam

3. Department of Chemistry, Faculty of Basic Science, Can Tho University of Medicine and Pharmacy, Vietnam

4. Institut de Chimie des Substances Naturelles, CNRS UPR 2301, Université Paris-Sud, Université Paris-Saclay, 1, av de la Terrasse, 91198 Gif-sur-Yvette, France

Abstract

Sodium sulfide trihydrate promoted-redox condensation of o-nitroanilines with α-tetralones to benzo[a]phenazines.

Funder

Vietnam Academy of Science and Technology

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2024/OB/D3OB02028B

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