Synthesis of Carboxylic Acids, Esters and Their Derivatives (1991)

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Science , — Bode, J. Zhang, Y. Protein chemical synthesis by serine and threonine ligation. Natl Acad. USA , — Nilsson, B. Staudinger ligation: a peptide from a thioester and azide. Noda, H. Rapid ligations with equimolar reactants in water with the potassium acyltrifluoroborate amide formation. Hydroxymethyl salicylaldehyde auxiliary for a glycine-dependent amide-forming ligation. Constable, D. Key green chemistry research areas: a perspective from pharmaceutical manufacturers.

Green Chem. Tamaru, Y.

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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.

Supplementary files

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.

Li, F. Combination of gold and iridium catalysts for the synthesis of N-alkylated amides from nitriles and alcohols. Miyamura, H. Size of gold nanoparticles driving selective amide synthesis through aerobic condensation of aldehydes and amines.

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.

Alcohol Preparation By Carboxylic Acid & its Derivative's Reduction with Mechanism

Chary, B. Gold I -catalyzed addition of carboxylic acids to alkynes. Rotem, M. Addition of carboxylic acids to alkynes catalyzed by ruthenium complexes. Vinyl ester formation.

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.

Kita, Y.

Description

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.

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