2009
DOI: 10.1016/j.jorganchem.2009.03.036
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Design of nickel chelates of tetradentate N-heterocyclic carbenes with subdued cytotoxicity

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Cited by 56 publications
(39 citation statements)
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“…In particular, the (533−534), [163] (535), [164] (536), [165] (543−544), [166] (545−546), [167] (548 [168]−557), [169] (558), [51] (559), [71] (560), [161] (561), [170] (562−563), [141] (565), [171] (566−567), [172] (568), [173] (569), [126d] (570−573), [174] (574), [175] (575−576), [176] (577), [177] (578), [178] (579), [106] (580−581), [179] (582−583), [151] (584−585), [180] (586−588), [181] (595−596), [182] (597−599), [183] (600−603), [184] (604), [185] (605−608), [186] (609), [185] (610−613), [187] (614−618), [188] (619−621), [189] (622−623), [185] (624−630), [190] (631), [191] (633−635), [192] (636), [193] (637), [194] (647) [195] and (648) [196] complexes were obtained by this pathway from the treatment of the free or the in situ generated NHC The third route is the oxidation method (Scheme 15) using which the (589−590), [197] (638) …”
Section: Neutral Chelated Ni(ii)−nhc Complexesmentioning
confidence: 99%
“…In particular, the (533−534), [163] (535), [164] (536), [165] (543−544), [166] (545−546), [167] (548 [168]−557), [169] (558), [51] (559), [71] (560), [161] (561), [170] (562−563), [141] (565), [171] (566−567), [172] (568), [173] (569), [126d] (570−573), [174] (574), [175] (575−576), [176] (577), [177] (578), [178] (579), [106] (580−581), [179] (582−583), [151] (584−585), [180] (586−588), [181] (595−596), [182] (597−599), [183] (600−603), [184] (604), [185] (605−608), [186] (609), [185] (610−613), [187] (614−618), [188] (619−621), [189] (622−623), [185] (624−630), [190] (631), [191] (633−635), [192] (636), [193] (637), [194] (647) [195] and (648) [196] complexes were obtained by this pathway from the treatment of the free or the in situ generated NHC The third route is the oxidation method (Scheme 15) using which the (589−590), [197] (638) …”
Section: Neutral Chelated Ni(ii)−nhc Complexesmentioning
confidence: 99%
“…With one of the ongoing theme of our research being in exploring the biomedical [26,27] and catalytic [28e41] potentials of N-heterocyclic carbene [42e47] complexes of transition metals, we became interested in constructing a variety of CeX (X ¼ C, heteroatom) bonds catalytically, including the base-free Michael reactions using bifunctional catalysts [48,49]. We rationalized that q Dedicated to Professor Christian Bruneau on his 60th birthday.…”
Section: Introductionmentioning
confidence: 99%
“…2, IV) [38e40] or the dianionic C * NNC * ligands (Fig. 2, V) [37,41] there have been (to the best of our knowledge) no reports of di(imidazol-2-ylidene) ligands with amide-functionalized side chains.…”
Section: Introductionmentioning
confidence: 99%