Academic literature on the topic 'Carbene N-Heterocyclic borane'

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Journal articles on the topic "Carbene N-Heterocyclic borane"

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Frogneux, Xavier, Laura Hippolyte, Dimitri Mercier, et al. "Direct Synthesis of N‐Heterocyclic Carbene‐Stabilized Copper Nanoparticles from an N‐Heterocyclic Carbene–Borane." Chemistry – A European Journal 25, no. 49 (2019): 11481–85. http://dx.doi.org/10.1002/chem.201901534.

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Pidlypnyi, Nazar, Jan C. Namyslo, Martin H. H. Drafz, Martin Nieger, and Andreas Schmidt. "Betaine–Carbene Interconversions. From N-Ylides to Zwitterionic N-Heterocyclic Carbene–Borane Adducts." Journal of Organic Chemistry 78, no. 3 (2013): 1070–79. http://dx.doi.org/10.1021/jo302479p.

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Winkler, Andrea, Matthias Freytag, Peter G. Jones, and Matthias Tamm. "Preparation and reactivity of an isolable N-heterocyclic carbene–borane." Journal of Organometallic Chemistry 775 (January 2015): 164–68. http://dx.doi.org/10.1016/j.jorganchem.2014.04.037.

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Banerjee, Dipshikha, Céline Besnard, and E. Peter Kündig. "Chiral N-Heterocyclic Carbene Borane Complexes: Synthesis and Structural Analysis." Organometallics 31, no. 2 (2012): 709–15. http://dx.doi.org/10.1021/om201087n.

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Korytiaková, Eva, Niklas O. Thiel, Felix Pape, and Johannes F. Teichert. "Copper(i)-catalysed transfer hydrogenations with ammonia borane." Chemical Communications 53, no. 4 (2017): 732–35. http://dx.doi.org/10.1039/c6cc09067b.

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Highly Z-selective alkyne transfer semihydrogenations and conjugate transfer hydrogenations of enoates can be effected by employing a readily available copper(i)/N-heterocyclic carbene (NHC) complex, [IPrCuOH], in combination with ammonia borane as a H<sub>2</sub> equivalent.
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Liu, Ming, Jan C. Namyslo, Martin Nieger, Mika Polamo, and Andreas Schmidt. "From betaines to anionic N-heterocyclic carbenes. Borane, gold, rhodium, and nickel complexes starting from an imidazoliumphenolate and its carbene tautomer." Beilstein Journal of Organic Chemistry 12 (December 8, 2016): 2673–81. http://dx.doi.org/10.3762/bjoc.12.264.

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The mesomeric betaine imidazolium-1-ylphenolate forms a borane adduct with tris(pentafluorophenyl)borane by coordination with the phenolate oxygen, whereas its NHC tautomer 1-(2-phenol)imidazol-2-ylidene reacts with (triphenylphosphine)gold(I) chloride to give the cationic NHC complex [Au(NHC)2][Cl] by coordination with the carbene carbon atom. The anionic N-heterocyclic carbene 1-(2-phenolate)imidazol-2-ylidene gives the complexes [K][Au(NHC−)2], [Rh(NHC−)3] and [Ni(NHC−)2], respectively. Results of four single crystal analyses are presented.
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Lamm, Vladimir, Xiangcheng Pan, Tsuyoshi Taniguchi, and Dennis P. Curran. "Reductions of aldehydes and ketones with a readily available N-heterocyclic carbene borane and acetic acid." Beilstein Journal of Organic Chemistry 9 (April 8, 2013): 675–80. http://dx.doi.org/10.3762/bjoc.9.76.

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Acetic acid promotes the reduction of aldehydes and ketones by the readily available N-heterocyclic carbene borane, 1,3-dimethylimidazol-2-ylidene borane. Aldehydes are reduced over 1–24 h at room temperature with 1 equiv of acetic acid and 0.5 equiv of the NHC-borane. Ketone reductions are slower but can be accelerated by using 5 equiv of acetic acid. Aldehydes can be selectively reduced in the presence of ketones. On a small scale, products are isolated by evaporation of the reaction mixture and direct chromatography.
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Bolt, Daniel A., and Dennis P. Curran. "1-Butyl-3-methylimidazol-2-ylidene Borane: A Readily Available, Liquid N-Heterocyclic Carbene Borane Reagent." Journal of Organic Chemistry 82, no. 24 (2017): 13746–50. http://dx.doi.org/10.1021/acs.joc.7b02730.

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Takahashi, Kosuke, Steven J. Geib, Katsuhiro Maeda, Dennis P. Curran, and Tsuyoshi Taniguchi. "Radical trans-Hydroboration of Substituted 1,3-Diynes with an N-Heterocyclic Carbene Borane." Organic Letters 23, no. 3 (2021): 1071–75. http://dx.doi.org/10.1021/acs.orglett.0c04284.

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Zhang, Jiaxi, Eike G. Hübner, Jan C. Namyslo, Martin Nieger, and Andreas Schmidt. "Purine-substituted imidazolium mesomeric betaines and their tautomeric N-heterocyclic carbenes. Formation of a cyclic borane adduct." Organic & Biomolecular Chemistry 16, no. 36 (2018): 6801–8. http://dx.doi.org/10.1039/c8ob01916a.

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Dissertations / Theses on the topic "Carbene N-Heterocyclic borane"

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Hippolyte, Laura. "New syntheses of N-heterocyclic carbene-stabilized gold nanoparticles." Electronic Thesis or Diss., Sorbonne université, 2018. https://accesdistant.sorbonne-universite.fr/login?url=https://theses-intra.sorbonne-universite.fr/2018SORUS148.pdf.

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Récemment, les carbènes N-hétérocycliques (NHC) ont suscité un intérêt important dans le domaine de la chimie des matériaux. En effet, cette nouvelle catégorie de ligands forme des liaisons très fortes avec une diversité de métaux et leur structure, ainsi que leurs propriétés électroniques, peuvent être adaptées par de la synthèse organique. Cette forte liaison est d’un intérêt particulier dans le domaine des nanoparticules d’or (NP) et des synthèses ont déjà été proposées. En effet, les NPs présentent de nombreuses applications potentielles, par exemple dans les capteurs, en catalyse ou médec
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Liu, Ming [Verfasser], and Andreas [Akademischer Betreuer] Schmidt. "Formation of borane adducts and some complexes starting from N-heterocyclic carbenes / Ming Liu ; Betreuer: Andreas Schmidt." Clausthal-Zellerfeld : Technische Universität Clausthal, 2017. http://d-nb.info/1231364963/34.

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Book chapters on the topic "Carbene N-Heterocyclic borane"

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"Product Subclass 42: N-Heterocyclic Carbene Borane Complexes." In Knowledge Updates 2014/4, edited by Banert, Hall, Joule, Moloney, Reissig, and Schaumann. Georg Thieme Verlag, 2015. http://dx.doi.org/10.1055/sos-sd-101-00511.

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