Issue 94, 2015

Direct access to pyrimidines through organocatalytic inverse-electron-demand Diels–Alder reaction of ketones with 1,3,5-triazine

Abstract

An organocatalytic inverse-electron-demand Diels–Alder reaction of ketones with 1,3,5-triazine through enamine catalysis has been developed. This method could furnish 4,5-disubstituted pyrimidines in good yields and high levels of regioselectivities.

Graphical abstract: Direct access to pyrimidines through organocatalytic inverse-electron-demand Diels–Alder reaction of ketones with 1,3,5-triazine

Supplementary files

Article information

Article type
Communication
Submitted
22 Aug 2015
Accepted
04 Sep 2015
First published
07 Sep 2015

RSC Adv., 2015,5, 76759-76763

Author version available

Direct access to pyrimidines through organocatalytic inverse-electron-demand Diels–Alder reaction of ketones with 1,3,5-triazine

G. Yang, Q. Jia, L. Chen, Z. Du and J. Wang, RSC Adv., 2015, 5, 76759 DOI: 10.1039/C5RA16995J

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