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Iminoiodane- and Bronsted base-mediated cross dehydrogenative coupling of cyclic ethers with 1,3-dicarbonyl compounds
Tejo C.3; Sim X.R.3; Lee B.R.1; Ayers B.J.3; Leung C.-H.5; Ma D.-L.2; Chan P.W.H.1
2015-07-01
Source PublicationMolecules
ISSN14203049
Volume20Issue:7Pages:13336-13353
Abstract

A one-pot, two-step approach to prepare 2-tetrahydrofuran and -pyran substituted 1,3-dicarbonyl compounds by PhI=NTs-mediated amination/Brønsted base-catalyzed cross dehydrogenative coupling (CDC) reaction of the cyclic ether and 1,3-dicarbonyl derivative under mild conditions is reported. The reaction is compatible with a variety of cyclic ethers and 1,3-dicarbonyl compounds, affording the corresponding coupled products in moderate to good yields of up to 80% over two steps.

Keyword1,3-dicarbonyl Compounds C-c Bond Formation Cross Dehydrogenation Coupling Iminoiodanes Metal-free Catalysis
DOI10.3390/molecules200713336
URLView the original
Indexed BySCIE
WOS Research AreaBiochemistry & Molecular Biology ; Chemistry
WOS SubjectBiochemistry & Molecular Biology ; Chemistry, Multidisciplinary
WOS IDWOS:000368695400102
Scopus ID2-s2.0-84938499540
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Document TypeJournal article
CollectionInstitute of Chinese Medical Sciences
Affiliation1.Monash University
2.Hong Kong Baptist University
3.Nanyang Technological University
4.The University of Warwick
5.University of Macau
Recommended Citation
GB/T 7714
Tejo C.,Sim X.R.,Lee B.R.,et al. Iminoiodane- and Bronsted base-mediated cross dehydrogenative coupling of cyclic ethers with 1,3-dicarbonyl compounds[J]. Molecules, 2015, 20(7), 13336-13353.
APA Tejo C.., Sim X.R.., Lee B.R.., Ayers B.J.., Leung C.-H.., Ma D.-L.., & Chan P.W.H. (2015). Iminoiodane- and Bronsted base-mediated cross dehydrogenative coupling of cyclic ethers with 1,3-dicarbonyl compounds. Molecules, 20(7), 13336-13353.
MLA Tejo C.,et al."Iminoiodane- and Bronsted base-mediated cross dehydrogenative coupling of cyclic ethers with 1,3-dicarbonyl compounds".Molecules 20.7(2015):13336-13353.
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