Abstract
An efficient and one-pot synthesis of 2,4,6-triarylpyridines by palladium-catalyzed cyclocondensation of benzaldehydes, terminal aromatic alkynes and ammonium bifluoride in the presence of tert-butyl peroxide (TBP) as oxidant is developed.
Keywords: Aromatic alkyne, ammonium bifluoride; benzaldehyde, cyclocondensation, triarylpyridines.
Current Organic Synthesis
Title:One-Pot Synthesis of 2,4,6-Triarylpyridines by the Oxidative Cyclocondensation of Benzaldehydes, Aromatic Alkynes and Ammonium Bifluoride
Volume: 10 Issue: 4
Author(s): Ping Wang, Ruimao Hua and Chao-Jun Li
Affiliation:
Keywords: Aromatic alkyne, ammonium bifluoride; benzaldehyde, cyclocondensation, triarylpyridines.
Abstract: An efficient and one-pot synthesis of 2,4,6-triarylpyridines by palladium-catalyzed cyclocondensation of benzaldehydes, terminal aromatic alkynes and ammonium bifluoride in the presence of tert-butyl peroxide (TBP) as oxidant is developed.
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Cite this article as:
Wang Ping, Hua Ruimao and Li Chao-Jun, One-Pot Synthesis of 2,4,6-Triarylpyridines by the Oxidative Cyclocondensation of Benzaldehydes, Aromatic Alkynes and Ammonium Bifluoride, Current Organic Synthesis 2013; 10 (4) . https://dx.doi.org/10.2174/157017941004150310102446
DOI https://dx.doi.org/10.2174/157017941004150310102446 |
Print ISSN 1570-1794 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6271 |
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