One-pot tandem hiyama alkynylation/cyclizations by palladium(II) acyclic diaminocarbene (ADC) complexes yielding biologically relevant benzofuran scaffolds

Chandan Singh, A.P. Prakasham, Manoj Kumar Gangwar, Raymond J. Butcher, Prasenjit Ghosh

Onderzoeksoutput: Bijdrage aan tijdschriftTijdschriftartikelAcademicpeer review

36 Citaten (Scopus)

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-2Engels
Pagina's (van-tot)1740-1756
Aantal pagina's17
TijdschriftACS Omega
Volume3
Nummer van het tijdschrift2
DOI's
StatusGepubliceerd - 9 feb. 2018
Extern gepubliceerdJa

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.

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