Philip Kraft, Walter Eichenberger, Georg Fráter. Get article recommendations from ACS based on references in your Mendeley library. Transannular Claisen rearrangement reactions for the synthesis of vinylcyclobutanes: formal synthesis of (±)-grandisol. Stereoselective Synthesis of Deuterium-Labeled (2S)-Cyclohexenyl Alanines, Biosynthetic Intermediates of Cinnabaramide. Reactions of 1,2-Diketones with Vinyllithium: Addition Reactions and Dianionic Oxy Cope Rearrangements of Cyclic and Acyclic Substrates. Total synthesis of (±)-isoavenaciolide and (±)-avenaciolide. The first total synthesis of (±)-lagopodin A. Damien Bourgeois, Donald Craig, Fabienne Grellepois, David M. Mountford, Alan J.W. Synthesis of 1,2‐Amino Alcohols by Sigmatropic Rearrangements of 3‐( meta Acids via a MeONa/LiCl-Mediated Sterically Hindered Claisen Condensation-Knorr Total synthesis of (±)-β-chamigrene and (±)-laurencenone C via Ireland ester Claisen rearrangement and an intramolecular type II carbonyl ene reaction sequence. Lett., Consecutive Michael-Claisen Process for Cyclohexane-1,3-dione Derivative (CDD) Ethanol can be excluded from your answer. List of Name Reaction of Organic Chemistry consist of detail Reaction Mechanism of all name reactions of Organic Chemistry. Legal. Steven D. Burke, Christopher J. O'Donnell, Jeremy J. Hans, Choong Woon Moon, Raymond A. Ng, Thomas W. Adkins, Garrick K. Packard. Oxyanionic Sigmatropic Rearrangements Relevant to Cyclooctadienone Formation in Penostatins I and F. Nathan W. G. Fairhurst, Mary F. Mahon, Rachel H. Munday, and David R. Carbery . R. R. Akhmetvaleev, L. R. Imaeva, T. A. Belogaeva, M. S. Miftakhov. Synthesis of "One-Pot" Synthesis of 4-Substituted 1,5-Diaryl-1H-pyrazole-3-carboxylic Palladium(0)-induzierte, enantiodivergente Alkylierung von Cyclopent-2-en-1,3-diol-Derivaten. Mechanism of the Claisen Rearrangement. Ireland-Claisen Rearrangement of 6-Methylene-1,4-oxazepan-2-ones. Divergent Total Synthesis of the Tricyclic Marine Alkaloids Lepadiformine, Fasicularin, and Isomers of Polycitorols by Reagent-Controlled Diastereoselective Reductive Amination. Serine-cis-proline and Serine-trans-proline Isosteres:  Stereoselective Synthesis of (Z)- and (E)-Alkene Mimics by Still−Wittig and Ireland−Claisen Rearrangements. Stereoselective Total Synthesis of (−)-Perrottetinene and Assignment of Its Absolute Configuration. -2-Methyl α- and β- Mitsuo Sado, Hideaki Abe, Nobuki Inuzuka, Kozo Shirai, Takanobu Kumamoto. Dominika Krištofíková, Juraj Filo, Mária Mečiarová, Radovan Šebesta. Total Synthesis of (+)-Suaveolindole:  Establishment of Its Absolute Configuration. Synthesis of Tubuphenylalanines via Ireland–Claisen Rearrangement. Total Synthesis of 3-Deoxy-d-manno-2-octulosonic Acid (KDO) and 2-Deoxy-β-KDO. different esters are used, an essentially statistical mixture of all Hans Jürgen Günther, Eberhard Guntrum, Volker Jäger. Synthesis of 2,2-Disubstituted Furanoid Natural Products:  Total Synthesis of Sphydrofuran. Amanda Sølvhøj, Esben Taarning, Robert Madsen. Organocatalytic Name Reactions Enabled by NHCs. -Butyldimethylchlorosilane. Post your questions about chemistry, whether they're school related or just out of general interest. Theory of Substituent Effects on Pericyclic Reaction Rates:  Alkoxy Substituents in the Claisen Rearrangement. A New Method for the Construction of Macrolides Stereoselective Synthesis of (±)-Phoracantholide J. Double decarboxylative Claisen rearrangement reactions: microwave-assisted de novo synthesis of pyridines. The Claisen condensation reaction is an organic coupling reaction that results in the formation of a C-C bond between either a single ester and one carbonyl compound or between two esters. Mingji Dai, Isaac J. Krauss and Samuel J. Danishefsky . The First Stereoselective Ficini−Claisen Rearrangement Using Chiral Ynamides. determine whether a given pair of esters is likely to produce a good yield of a single product when subjected to a mixed Claisen condensation.

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