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26 Apr 2010 A Versatile and Efficient Palladium- meta -Terarylphosphine Catalyst for the Copper-Free Sonogashira Coupling of (Hetero-)Aryl Chlorides and Alkynes. Yong Yang , Xinying Chew , Charles W. Johannes , Edward G. Robins , Howard Jong , Yee Hwee Lim. European Journal of Organic Chemistry 2014
Niko Bonatsos is a managing director at General Catalyst, a venture capital firm with offices in San Francisco, Palo Alto, New York and appr Partner Investments. Number of Partner Investments 6. Announced Date. Organization Name. Investor Name. Lead Investor. Funding Round. Money Raised. Mar 16, 2017. Livongo.
3 Dec 2014 In a very recent article (Chem.—Eur. J. 2014, 20, 6636), Olson et al. performed a theoretical study of the low-lying isomers of Li3N3 and found that two of the most stable structures show a novel N33– molecular motif, which possesses structural and chemical bonding features similar to ozone. We explore a
17 Nov 2010 Mechanistic Insight into Catalyst-Transfer Polymerization of Unusual Anion-Radical Naphthalene Diimide Monomers: An Observation of Ni(0) Intermediates. Volodymyr Senkovskyy , Roman Tkachov , Hartmut Komber , Andreas John , Jens-Uwe Sommer , and Anton Kiriy. Macromolecules 2012 45 (19),
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17 Nov 2017 Transition-metal-catalyzed N–H insertion of a diazocarbonyl compound is applied for polycondensation for the first time to give a new type of aromatic polyamine. The well-defined polyamines were obtained by [RuCl2(p-cymene)]2-catalyzed reaction of diethyl 1,4-phenylenebis(diazoacetate) with dianilines
28 Sep 2015 An efficient and convenient procedure that generates the active Ni(0) catalyst in situ from cheap, air stable Ni(II) precursors is developed for the [4 + 2]-cycloaddition of alkynes and 3-azetidinones. The reaction affords useful 3-dehydropiperidinones in comparable yields to the reported Ni(0) procedure.
6 Jun 1996 The consequences of deactivation on FCC catalyst activity and selectivity are reviewed and possible relations between the various deactivation phenomena are qualitatively indicated. A few cases of FCC catalyst deactivation are highlighted, specifically addressing the question how to simulate the
7 Aug 2013 Highly atroposelective Meyers' lactamization promoted by pivalic acid under microwave irradiation is reported which allows the construction of nonracemic substituted-dibenzo(di)azepine derivatives through a center to axial chirality transfer principle, controlling the otherwise configurationally labile biaryl
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