Stereoelectronic effects in ring closure reactions
- 1 January 1983
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 24 (28) , 2851-2854
- https://doi.org/10.1016/s0040-4039(00)88041-7
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Base-catalysed cyclisation of N-alkyl-(Tetrahedron Letters, 1983
- A critical test of the theory of stereoelectronic controlJournal of the American Chemical Society, 1982
- Reversal of electronic effects between inter- and intra-molecular Michael addition reactionsJournal of the Chemical Society, Chemical Communications, 1982
- The kinetics and mechanism of the cyclisation of some 2′-hydroxychalcones to flavanones in basic aqueous solutionJournal of the Chemical Society, Perkin Transactions 2, 1982
- Intramolecullar alkylation of phenols. Part 4. Base-catalysed cyclisation of phenolic enones. Scope and limitationsJournal of the Chemical Society, Perkin Transactions 1, 1980
- Rules for ring closure: ring formation by conjugate addition of oxygen nucleophilesThe Journal of Organic Chemistry, 1977
- Friedel-crafts cyclisation—VI11Part V.J.M. Allen, K.M. Johnston and R.G. Shotter, Chem. & Ind. 108 (1976).Tetrahedron, 1977
- Preference for 6-Exo-Trigonal closures of ω-hydroxy-αβ-unsaturated estersJournal of the Chemical Society, Chemical Communications, 1977
- Rules for ring closureJournal of the Chemical Society, Chemical Communications, 1976
- Stereoelectronic control in the cleavage of tetrahedral intermediates in the hydrolysis of esters and amidesTetrahedron, 1975