Samenvatting
A series of palladium acyclic diaminocarbene (ADC) complexes of the type cis-[(R1NH)(R2)methylidene]- PdCl2(CNR1) [R1 = 2, 4, 6-(CH3)3C6H2: R2 = NC5 H10 (2); NC4H8 (3); NC4H8O (4)] were used not only to perform the Csp2-Csp Hiyama coupling between aryl iodide and triethoxysilylalkynes but also to subsequently carry out the one-pot tandem Hiyama alkynylation/cyclization reaction between 2- iodophenol and triethoxysilylalkynes, giving a convenient timeefficient access to the biologically relevant benzofuran compounds. The palladium ADC complexes (2-4) were conveniently synthesized by the nucleophilic addition of secondary amines, namely, piperidine, pyrrolidine, and morpholine on the cis-{(2, 4, 6-(CH3)3C6H2)NC}2PdCl2 in moderate yields (ca. 61-66%) .
Originele taal-2 | Engels |
---|---|
Pagina's (van-tot) | 1740-1756 |
Aantal pagina's | 17 |
Tijdschrift | ACS Omega |
Volume | 3 |
Nummer van het tijdschrift | 2 |
DOI's | |
Status | Gepubliceerd - 9 feb. 2018 |
Extern gepubliceerd | Ja |
Bibliografische nota
Publisher Copyright:© 2018 American Chemical Society.
Financiering
We thank the Department of Science and Technology (EMR/ 2014/000254), New Delhi, India, for financial support of this research. We gratefully acknowledge Single Crystal X-ray Diffraction Facility, Department of Chemistry, IIT Bombay, Mumbai, India, for the crystallographic characterization data. C.S., A.P.P. and M.K.G., thank CSIR, New Delhi, India, for research fellowships.