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      A Broadly Applicable Strategy for Entry into Homogeneous Nickel(0) Catalysts from Air-Stable Nickel(II) Complexes

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          Abstract

          A series of air-stable nickel complexes of the form L 2Ni(aryl) X (L = monodentate phosphine, X = Cl, Br) and LNi(aryl)X (L = bis-phosphine) have been synthesized and are presented as a library of precatalysts suitable for a wide variety of nickel-catalyzed transformations. These complexes are easily synthesized from low-cost NiCl 2·6H 2O or NiBr 2·3H 2O and the desired ligand followed by addition of 1 equiv of Grignard reagent. A selection of these complexes were characterized by single-crystal X-ray diffraction, and an analysis of their structural features is provided. A case study of their use as precatalysts for the nickel-catalyzed carbonyl-ene reaction is presented, showing superior reactivity in comparison to reactions using Ni(cod) 2. Furthermore, as the precatalysts are all stable to air, no glovebox or inert-atmosphere techniques are required to make use of these complexes for nickel-catalyzed reactions.

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          Nickel-catalyzed cross-couplings involving carbon-oxygen bonds.

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            Is Open Access

            Exploiting the Brønsted Acidity of Phosphinecarboxamides for the Synthesis of New Phosphides and Phosphines

            We demonstrate that the synthesis of new N-functionalized phosphinecarboxamides is possible by reaction of primary and secondary amines with PCO− in the presence of a proton source. These reactions proceed with varying degrees of success, and although primary amines generally afford the corresponding phosphinecarboxamides in good yields, secondary amines react more sluggishly and often give rise to significant decomposition of the 2-phosphaethynolate precursor. Of the new N-derivatized phosphinecarboxamides available, PH2C(O)NHCy (Cy=cyclohexyl) can be obtained in sufficiently high yields to allow for the exploration of its Brønsted acidity. Thus, deprotonating PH2C(O)NHCy with one equivalent of potassium bis(trimethylsilyl)amide (KHMDS) gave the new phosphide [PHC(O)NHCy]−. In contrast, deprotonation with half of an equivalent gives rise to [P{C(O)NHCy}2]− and PH3. These phosphides can be employed to give new phosphines by reactions with electrophiles, thus demonstrating their enormous potential as chemical building blocks.
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              Development of an air-stable nickel precatalyst for the amination of aryl chlorides, sulfamates, mesylates, and triflates.

              A new air-stable nickel precatalyst for C-N cross-coupling is reported. The developed catalyst system displays a greatly improved substrate scope for C-N bond formation to include both a wide range of aryl and heteroaryl electrophiles and aryl, heteroaryl, and alkylamines. The catalyst system is also compatible with a weak base, allowing the amination of substrates containing base-sensitive functional groups.
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                Author and article information

                Journal
                Organometallics
                Organometallics
                om
                orgnd7
                Organometallics
                American Chemical Society
                0276-7333
                1520-6041
                16 April 2015
                16 April 2014
                28 April 2014
                : 33
                : 8
                : 2012-2018
                Affiliations
                [1]Department of Chemistry, Massachusetts Institute of Technology , Cambridge, Massachusetts 02139, United States
                Author notes
                [* ]E-mail for T.F.J.: tfj@ 123456mit.edu .
                Article
                10.1021/om500156q
                4006606
                24803717
                f34db186-96de-445b-b596-c0c35c46b887
                Copyright © 2014 American Chemical Society
                History
                : 12 February 2014
                Funding
                National Institutes of Health, United States
                Categories
                Article
                Custom metadata
                om500156q
                om-2014-00156q

                Inorganic & Bioinorganic chemistry
                Inorganic & Bioinorganic chemistry

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