JP Djukic, JB Sortais, L Barloy… - European Journal of …, 2009 - Wiley Online Library
The syntheses of cycloruthenated compounds by several methods, and especially by the C– H activation pathway, have been reviewed. Many ruthenium‐containing starting materials …
S Inoue, H Shiota, Y Fukumoto… - Journal of the American …, 2009 - ACS Publications
A new type of carbonylation of the ortho C− H bonds in aromatic amides 1, in which the pyridin-2-ylmethylamino moiety functions as a bidentate directing group, can be achieved …
A general catalytic hydrogen transfer‐mediated α‐functionalization of 1, 8‐naphthyridines is reported for the first time that benefits from a hydrogen transfer‐mediated activation mode for …
B Saha, SM Wahidur Rahaman, P Daw… - … A European Journal, 2014 - Wiley Online Library
Metal metal singly‐bonded diruthenium complexes, bridged by naphthyridine‐ functionalized N‐heterocyclic carbene (NHC) ligands featuring a hydroxy appendage on the …
RK Das, B Saha, SMW Rahaman… - Chemistry–A European …, 2010 - Wiley Online Library
Dipalladium (I) and diruthenium (I) compounds bridged by two [{(5, 7‐dimethyl‐1, 8‐ naphthyridin‐2‐yl) amino} carbonyl] ferrocene (L) ligands have been synthesized. The X‐ray …
The catalytic utility of [RuL1 (CO) 2I2](1), containing an annelated π-conjugated imidazo- naphthyridine-based mesoionic carbene (MIC) ligand (L1), is evaluated for E-selective …
A Sinha, SM Wahidur Rahaman, M Sarkar… - Inorganic …, 2009 - ACS Publications
The 1, 8-naphthyridine− functionalized N-heterocyclic carbene 1-benzyl-3-(5, 7-dimethyl-1, 8-naphthyrid-2-yl) imidazol-2-ylidene (BIN) has been successfully coordinated to Pd (II), W …
Pd-or Ni-catalyzed C–H arylation of 4-nitroimidazole derivatives directed by a manipulable nitro group was developed. The reaction tolerates a wide range of substituted aryl halides …
I Omae - Journal of Organometallic Chemistry, 2011 - Elsevier
Cyclometalation reactions proceed very easily with one step reaction between metal compounds and substrates having a heteroatom such as O, S, N, P and As. However, under …