Issue 52, 2020, Issue in Progress

ortho-Naphthoquinone-catalyzed aerobic oxidation of amines to fused pyrimidin-4(3H)-ones: a convergent synthetic route to bouchardatine and sildenafil

Abstract

A facile access to fused pyrimidin-4(3H)-one derivatives has been established by using the metal-free ortho-naphthoquinone-catalyzed aerobic cross-coupling reactions of amines. The utilization of two readily available amines allowed a direct coupling strategy to quinazolinone natural product, bouchardatine, as well as sildenafil (Viagra™) in a highly convergent manner.

Graphical abstract: ortho-Naphthoquinone-catalyzed aerobic oxidation of amines to fused pyrimidin-4(3H)-ones: a convergent synthetic route to bouchardatine and sildenafil

Supplementary files

Article information

Article type
Paper
Submitted
07 Aug 2020
Accepted
14 Aug 2020
First published
21 Aug 2020
This article is Open Access
Creative Commons BY license

RSC Adv., 2020,10, 31101-31105

ortho-Naphthoquinone-catalyzed aerobic oxidation of amines to fused pyrimidin-4(3H)-ones: a convergent synthetic route to bouchardatine and sildenafil

K. Kim, H. Y. Kim and K. Oh, RSC Adv., 2020, 10, 31101 DOI: 10.1039/D0RA06820A

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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