Preference conformationnelle dans l 'etat de transition. Application a la reduction de cetones par LiA1H4.
- 31 December 1972
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 13 (21) , 2153-2156
- https://doi.org/10.1016/s0040-4039(01)84792-4
Abstract
No abstract availableThis publication has 15 references indexed in Scilit:
- The structure of the transition state in nucleophilic addition reactions to carbonyl compounds.Tetrahedron Letters, 1970
- Reduction with metal hydrides—XIXTetrahedron, 1970
- Adamantanone : A model to assess the position of the transition state in nucleophilic addition reactions to carbonyl compounds.Tetrahedron Letters, 1970
- Transition state analysis: evidence against product development control in the sodium borohydride reduction of ketonesJournal of the Chemical Society D: Chemical Communications, 1970
- Barrier to the inversion of six-membered rings containing an sp2-hybridized carbonJournal of the American Chemical Society, 1968
- Torsional strain involving partial bonds. The stereochemistry of the lithium aluminium hydride reduction of some simple open-chain ketonesTetrahedron Letters, 1968
- Conformational effects in compounds with six-membered rings—IVTetrahedron, 1964
- Evidence for Parallel Control of Reaction Rate and Stereochemistry via the Electrostatic Influence of Remote Substituent DipolesJournal of the American Chemical Society, 1962
- Polar and solvent effects in the reduction of substituted cyclohexanonesTetrahedron Letters, 1961
- The Stereochemistry of Hydride ReductionsJournal of the American Chemical Society, 1956