The uncatalyzed Claisen rearrangement of chorismate to prephenate prefers a transition state of chair-like geometry
- 1 September 1985
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 107 (18) , 5306-5308
- https://doi.org/10.1021/ja00304a064
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Secondary tritium isotope effects as probes of the enzymic and nonenzymic conversion of chorismate to prephenateBiochemistry, 1983
- The fate of the hydrogens of phosphoenolpyruvate in the reaction catalyzed by 5-enolpyruvylshikimate-3-phosphate synthase. Isotope effects and isotope exchange.Journal of Biological Chemistry, 1982
- Stereochemical study of the [3,3] sigmatropic rearrangement of 1,5-diene-3-alkoxides. Application to the stereoselective synthesis of (.+-.)-juvabioneJournal of the American Chemical Society, 1980
- Molecular Orbital Studies of Enzyme Catalysed Reactions. Rearrangement of Chorismate to PrephenateAustralian Journal of Chemistry, 1979
- Stereospecificity of Phenylyruvate TautomeraseEuropean Journal of Biochemistry, 1977