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Green Chem. Tamaru, Y.
Direct oxidative transformation of aldehydes to amides by palladium catalysis. Tillack, A. Catalytic amination of aldehydes to amides.
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Yoo, W. Highly efficient oxidative amidation of aldehydes with amine hydrochloride salts. Gunanathan, C. Direct synthesis of amides from alcohols and amines with liberation of H2. Ekoue-Kovi, K. One-pot oxidative esterification and amidation of aldehydes. Dobereiner, G. Dehydrogenation as a substrate-activating strategy in homogeneous transition-metal catalysis. De Sarkar, S. Oxidative amidation and azidation of aldehydes by NHC catalysis. Chen, C.
Oxidative amide synthesis directly from alcohols with amines. Zhang, L.
Kang, B. Ruthenium-catalyzed redox-neutral and single-step amide synthesis from alcohol and nitrile with complete atom economy.
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Malonic Ester Synthesis
Owston, N. Iridium-catalyzed conversion of alcohols into amides via oximes. Bruneau C. Ishino, Y. Novel synthesis of enol esters through silver-catalyzed reaction of acetylenic compounds with carboxylic acids.
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A General Alkyl-Alkyl Cross-Coupling Enabled by Redox-Active Esters and Alkylzinc Reagents
Organometallics 2 , — Mitsudo, T. Selective addition of unsaturated carboxylic acids to terminal acetylenes catalyzed by bis. A novel synthesis of enol esters. Ruppin, C. Regioselective synthesis of isopropenyl esters by ruthenium catalysed addition of N-protected amino-acids to propyne. Bruneau, C. Ruthenium-catalysed additions to alkynes: synthesis of activated esters and their use in acylation reactions. Synlett , — Regiocontrolled ru-catalyzed addition of carboxylic acids to alkynes: practical protocols for the synthesis of vinyl esters.
Facile and efficient syntheses of carboxylic anhydrides and amides using trimethylsilyl ethoxyacetylene. Kabouche, Z. Enol esters as intermediates for the facile conversion of amino acids into amides and dipeptides. Neveux, M. Novel syntheses of oxamides, oxamates and oxalates from diisopropenyl oxalate. Tetrahedron 49 , — Selective transformations of alkynes with ruthenium catalysts.
Perkin Trans. Racemization-free chemoenzymatic peptide synthesis enabled by the ruthenium-catalyzed synthesis of peptide enol esters via alkyne-addition and subsequent conversion using alcalase-cross-linked enzyme aggregates. Ashton Acton, Q. Doucet, H. General synthesis of Z -alkenyl esters via ruthenium-catalyzed anti-Markovnikov trans-addition of carboxylic acids to terminal alkynes. Stereoselective synthesis of Z-enol esters catalysed by [bis diphenylphosphino alkane]bis 2-methylpropenyl ruthenium complexes.
Synthesis of secondary enamides by ruthenium-catalyzed selective addition of amides to terminal alkynes.
- Synthesis of carboxylic acids, esters, and their derivatives in SearchWorks catalog.
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Cadierno, V. Ruthenium IV -catalyzed Markovnikov addition of carboxylic acids to terminal alkynes in aqueous medium. Organometallics 30 , — Alonso, F. Download references. Correspondence to Lukas J. This work is licensed under a Creative Commons Attribution 4.
Thieme E-Journals - Synlett / Abstract
Reprints and Permissions. RSC Advances Green Chemistry Applied Organometallic Chemistry Tetrahedron Letters By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate. Advanced search. Skip to main content. Subjects Catalyst synthesis Chemical bonding Organic chemistry. Mechanism Malonic ester synthesis consists of four consecutive reactions that can be carried out in the same pot.
Mechanism 1 Saponification 2 Decarboxylation 3 Tautomerization All of the steps together form the Malonic ester synthesis. Hoogenboom , Phillip J. Ihrig , Arne N. Langsjoen , Carol J.