Correction for 'On the mercuration, palladation, transmetalation and direct auration of a C^N^C pincer ligand' by Alice Jane McEllin , , 2023, , 872-876, https://doi.org/10.1039/d2dt04114f.
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Dalton Trans
April 2024
Department of Chemistry, University of York, Heslington, YORK YO10 5DD, UK.
Correction for 'On the mercuration, palladation, transmetalation and direct auration of a C^N^C pincer ligand' by Alice Jane McEllin , , 2023, , 872-876, https://doi.org/10.1039/d2dt04114f.
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January 2023
Department of Chemistry, University of York, Heslington, YORK YO10 5DD, UK.
The C^N^C ligand 2,6-bis(2,3-dialkoxyphenyl)pyridine forms dimercury and orthopalladated complexes, both of which may be transmetallated to gold(III) complexes; the gold complexes may also be formed directly in a Rh(III)-catalysed process, hence it is possible to circumvent the use of organomercury intermediates in the synthesis of this important class of compound.
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December 2012
School of Chemical Sciences, University of Auckland, Private Bag 92019, Auckland 1142, New Zealand.
Treatment of N(2),N(6)-bis(6-acrylamidopyridin-2-yl)pyridine-2,6-dicarboxamide with benzimidazole gives the acyclic aza-Michael addition product N(2),N(6)-bis(6-(3-(1H-benzo[d]imidazol-1-yl)propanamido)pyridin-2-yl)pyridine-2,6-dicarboxamide (2). The macrocycle N(1),N(7)-pyridine-2,6-dimethyl-N(2),N(6)-bis(6-(3-(1H-benzo[d]imidazol-1-yl)propanamido)pyridin-2-yl)pyridine-2,6-dicarboxamide dibromide ([H(2)L(2)]Br(2)) is formed through the double alkylation of 2 with 2,6-bis(bromomethyl)pyridine. The imidazole analogues of 2 and [H(2)L(2)]Br(2) (1 and [H(2)L(1)]Br(2), respectively) have also been prepared.
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