The stereoselectivity of representative cyclobutenes in (4+2)π cycloaddition reactions
- 31 December 1970
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 11 (32) , 2735-2738
- https://doi.org/10.1016/s0040-4039(01)98326-1
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- The synthetic potential of the 1,2-photoaromatization (1) reactionTetrahedron Letters, 1969
- The Conservation of Orbital SymmetryAngewandte Chemie International Edition in English, 1969
- Stereochemistry of the Diels-Alder reaction. syn-anti IsomerismJournal of the American Chemical Society, 1969
- Diels–Alder reactions of the para-bonded valence isomer of hexafluorobenzene and of the benzvalene isomer of hexakis(trifluoromethyl)benzene: pyrrole as a dieneJournal of the Chemical Society D: Chemical Communications, 1969
- Reaction-path selectivity : cage formation versus photodechlorination in some alicyclic systems.Tetrahedron Letters, 1968
- Singlet and triplet states in cycloaddition to conjugated dienesPublished by Walter de Gruyter GmbH ,1968
- Tetrahedron Letters, 1967
- On the Nature of the Ground State of CyclobutadieneJournal of the American Chemical Society, 1966
- Diels-Alder Reactions of 3,3,4,4-Tetrafluorocyclobutene. Syntheses of Some Fluorinated BenzocyclobutenesThe Journal of Organic Chemistry, 1962
- Stereochemistry of the Diels-Alder Reaction.Chemical Reviews, 1961