Issue 8, 2014

Synthesis of 2-substituted pyrimidines and benzoxazoles via a visible-light-driven organocatalytic aerobic oxidation: enhancement of the reaction rate and selectivity by a base

Abstract

An efficient visible-light-driven photocatalytic oxidation of various 2-substituted dihydropyrimidines and phenolic imines has been achieved using an organic photocatalyst eosin Y bis(tetrabutyl ammonium salt) (TBA-eosin Y) and inexpensive oxidant molecular oxygen. With the aid of a base, significantly enhanced photoinduced electron transfer from substrates dihydropyrimidines or phenolic imines to the excited state of TBA-eosin Y has enabled the aerobic oxidation to yield 2-(methylthio)pyrimidines or 2-arylbenzoxazoles selectively.

Graphical abstract: Synthesis of 2-substituted pyrimidines and benzoxazoles via a visible-light-driven organocatalytic aerobic oxidation: enhancement of the reaction rate and selectivity by a base

Supplementary files

Article information

Article type
Communication
Submitted
24 Feb 2014
Accepted
14 Jun 2014
First published
18 Jun 2014

Green Chem., 2014,16, 3752-3757

Synthesis of 2-substituted pyrimidines and benzoxazoles via a visible-light-driven organocatalytic aerobic oxidation: enhancement of the reaction rate and selectivity by a base

L. Wang, Z. Ma, X. Wei, Q. Meng, D. Yang, S. Du, Z. Chen, L. Wu and Q. Liu, Green Chem., 2014, 16, 3752 DOI: 10.1039/C4GC00337C

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