Issue 5, 2021

Synthesis of spiro(indoline-2,3′-hydropyridazine) via an “on-water” [4 + 2] annulation reaction

Abstract

An on-water [4 + 2] annulation reaction between the 2-methyl-3H-indolium salt and α-bromo N-acyl hydrazone has been developed. The environmentally friendly strategy provides the first facile access to spiro(indoline-2,3′-hydropyridazine) scaffolds. Compared with the reaction in organic solvents, the use of water as the sole solvent remarkably improves the reaction efficiency as well as chemoselectivity. This green protocol features high yield, broad substrate scope, and mild reaction conditions.

Graphical abstract: Synthesis of spiro(indoline-2,3′-hydropyridazine) via an “on-water” [4 + 2] annulation reaction

Supplementary files

Article information

Article type
Research Article
Submitted
14 Nov 2020
Accepted
21 Dec 2020
First published
22 Dec 2020

Org. Chem. Front., 2021,8, 922-927

Synthesis of spiro(indoline-2,3′-hydropyridazine) via an “on-water” [4 + 2] annulation reaction

W. Zuo, J. Zhou, Y. Wu, H. Fang, X. Lang, Y. Li, G. Zhan and B. Han, Org. Chem. Front., 2021, 8, 922 DOI: 10.1039/D0QO01422B

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements