Iminonaphthofuranone synthesis via multiple-component cyclization of 2-naphthols using only molecular oxygen

Abstract

A multiple-component oxidative cyclization of easily available 2-naphthols, anilines, and ethyl glyoxylate is successfully achieved using only molecular oxygen. The reaction enables green, efficient and highly selective synthesis of iminonaphthofuranones, a category of disperse dyes that are previously inaccessible. The products exhibit a wide spectrum of colors, adjustable from pale orange to dark purple. They are also readily transformed into naphthofuranones and highly functionalized naphthols.

Graphical abstract: Iminonaphthofuranone synthesis via multiple-component cyclization of 2-naphthols using only molecular oxygen

Supplementary files

Article information

Article type
Research Article
Submitted
16 okt 2024
Accepted
12 dec 2024
First published
13 dec 2024

Org. Chem. Front., 2025, Advance Article

Iminonaphthofuranone synthesis via multiple-component cyclization of 2-naphthols using only molecular oxygen

J. Dong, S. Wu, L. Liu, D. Zhou, M. Mo, Y. Gao, L. Su, S. Yin and Y. Zhou, Org. Chem. Front., 2025, Advance Article , DOI: 10.1039/D4QO01939C

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