Search Results - "Madsen, Robert"
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Dehydrogenative Synthesis of Imines from Alcohols and Amines Catalyzed by a Ruthenium N-Heterocyclic Carbene Complex
Published in Organometallics (09-01-2012)“…A new method for the direct synthesis of imines from alcohols and amines is described where hydrogen gas is liberated. The reaction is catalyzed by the…”
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Silver‐Catalyzed Dehydrogenative Synthesis of Carboxylic Acids from Primary Alcohols
Published in Chemistry : a European journal (04-09-2017)“…A simple silver‐catalyzed protocol has been developed for the acceptorless dehydrogenation of primary alcohols into carboxylic acids and hydrogen gas. The…”
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Molybdenum‐Catalyzed Dehydrogenative Synthesis of Imines from Alcohols and Amines
Published in ChemCatChem (07-09-2018)“…A molybdenum N‐heterocyclic carbene catalyst has been developed for the synthesis of imines from primary alcohols and amines with the liberation of dihydrogen…”
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Ruthenium‐Catalyzed Dehydrogenative Decarbonylation of Primary Alcohols
Published in European journal of organic chemistry (02-10-2017)“…Dehydrogenative decarbonylation of a primary alcohol involves the release of both dihydrogen and carbon monoxide to afford the by one carbon unit shorter…”
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Dehydrogenative Synthesis of Carboxylic Acids from Primary Alcohols and Hydroxide Catalyzed by a Ruthenium N‑Heterocyclic Carbene Complex
Published in Journal of organic chemistry (21-10-2016)“…Primary alcohols have been reacted with hydroxide and the ruthenium complex [RuCl2(IiPr)(p-cymene)] to afford carboxylic acids and dihydrogen. The…”
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Development and mechanistic investigation of the manganese(iii) salen-catalyzed dehydrogenation of alcohols
Published in Chemical science (Cambridge) (2019)“…The first example of a manganese(iii) catalyst for the acceptorless dehydrogenation of alcohols is presented. ,…”
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Amide Synthesis from Alcohols and Amines Catalyzed by Ruthenium N-Heterocyclic Carbene Complexes
Published in Chemistry : a European journal (18-06-2010)“…The direct synthesis of amides from alcohols and amines is described with the simultaneous liberation of dihydrogen. The reaction does not require any…”
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Human and environmental impacts on river sediment microbial communities
Published in PloS one (19-05-2014)“…Sediment microbial communities are responsible for a majority of the metabolic activity in river and stream ecosystems. Understanding the dynamics in community…”
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Modern methods for shortening and extending the carbon chain in carbohydrates at the anomeric center
Published in Tetrahedron (18-11-2011)“…Recent advances in the cleavage and formation of C–C bonds at the anomeric center of carbohydrates are reviewed. Both chemical and enzymatic transformations…”
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The Mechanism for the Rhodium-Catalyzed Decarbonylation of Aldehydes: A Combined Experimental and Theoretical Study
Published in Journal of the American Chemical Society (16-04-2008)“…The mechanism for the rhodium-catalyzed decarbonylation of aldehydes was investigated by experimental techniques (Hammett studies and kinetic isotope effects)…”
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Experimental and Theoretical Mechanistic Investigation of the Iridium-Catalyzed Dehydrogenative Decarbonylation of Primary Alcohols
Published in Journal of the American Chemical Society (21-01-2015)“…The mechanism for the iridium–BINAP catalyzed dehydrogenative decarbonylation of primary alcohols with the liberation of molecular hydrogen and carbon monoxide…”
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Chemicals from Renewables: Aerobic Oxidation of Furfural and Hydroxymethylfurfural over Gold Catalysts
Published in ChemSusChem (22-02-2008)“…Aerobic exercise: The biomass‐derived platform chemicals furfural and hydroxymethylfurfural (HMF) are readily oxidized in methanol in the presence of oxygen…”
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Stannylene-Mediated Regioselective 6-O-Glycosylation of Unprotected Phenyl 1-Thioglycopyranosides
Published in European journal of organic chemistry (01-05-2013)“…A straightforward procedure is described for the synthesis of (1→6)‐linked saccharides by regioselective glycosylation of unprotected glycosyl acceptors…”
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A General and Convenient Method for the Rhodium-Catalyzed Decarbonylation of Aldehydes
Published in Advanced synthesis & catalysis (01-10-2006)“…A practical protocol for the decarbonylation of a wide range of aldehydes has been developed by using commercially available RhCl3⋅3 H2O and dppp in a diglyme…”
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Palladium-Catalyzed Aryl Amination-Heck Cyclization Cascade: A One-Flask Approach to 3-Substituted Indoles
Published in Angewandte Chemie (International ed.) (01-01-2008)“…Two for the price of one: A Pd/dppf‐based catalyst provides access to the title compounds from 1,2‐dihalogenated aromatic compounds and allylic amines in a…”
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Kinetic and Mechanistic Study of Aldose Conversion to Functionalized Furans in Aqueous Solutions
Published in Catalysts (01-03-2024)“…Reaction mixtures of naturally abundant aldoses and CH nucleophiles allow for the formation of functionalized furan precursors using low temperatures and…”
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Rhodium-Catalyzed Decarbonylation of Aldoses
Published in Journal of organic chemistry (07-12-2007)“…A catalytic procedure is described for decarbonylation of unprotected aldoses to afford alditols with one less carbon atom. The reaction is performed with the…”
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Enzymatic degradation of lignin-carbohydrate complexes (LCCs): Model studies using a fungal glucuronoyl esterase from Cerrena unicolor
Published in Biotechnology and bioengineering (01-05-2015)“…ABSTRACT Lignin‐carbohydrate complexes (LCCs) are believed to influence the recalcitrance of lignocellulosic plant material preventing optimal utilization of…”
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Investigation of Lipid Oxidation in the Raw Materials of a Topical Skin Formulation: A Topical Skin Formulation Containing a High Lipid Content
Published in Journal of the American Oil Chemists' Society (01-02-2018)“…Several studies have demonstrated that lipid oxidation often occurs in topical skin formulations which can affect product odor (both positively and…”
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Synthetic Applications and Mechanistic Studies of the Hydroxide-Mediated Cleavage of Carbon–Carbon Bonds in Ketones
Published in Journal of organic chemistry (02-06-2017)“…The hydroxide-mediated cleavage of ketones into alkanes and carboxylic acids has been reinvestigated and the substrate scope extended to benzyl carbonyl…”
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