Hammett-correlations, solvent effects and stereochemistry of the thermal decarboxylation of 2-oxetanones - evidence for a zwitterionic intermediate
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference15 articles.
1. Substituent effects on the preparations and thermal decarboxylations of .beta.-lactones derived from the cycloaddition of dichloroketene with monosubstituted benzaldehydes
2. Electronic effects exerted in the thermolysis of 2-oxetanone: Hammett studies of the 3-aryl and 4-aryl derivatives
3. threo-3-Hydroxycarboxylic acids as key intermediates in a highly stereoselective synthesis of (Z)- and (E)-olefins and enol ethers
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1. Mechanistic Insights into Ring-Opening and Decarboxylation of 2-Pyrones in Liquid Water and Tetrahydrofuran;Journal of the American Chemical Society;2013-04-09
2. NHC-Promoted Asymmetric β-Lactone Formation from Arylalkylketenes and Electron-Deficient Benzaldehydes or Pyridinecarboxaldehydes;The Journal of Organic Chemistry;2013-03-11
3. Synthetic and Quantum Mechanical Studies into the N-Heterocyclic Carbene Catalyzed (4 + 2) Cycloaddition;The Journal of Organic Chemistry;2012-01-06
4. A New Ring Expansion for a Chiral Hexahydroazulene Skeleton Possessing an Angular Methyl Group;The Journal of Organic Chemistry;2011-07-13
5. References;Solvents and Solvent Effects in Organic Chemistry;2010-11-26
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