The “syn-effect” in sulfines and carbonyl oxides: Conformational preferences of CH3CHSO and CH3CHOO
- 31 December 1981
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 22 (1) , 29-32
- https://doi.org/10.1016/0040-4039(81)80032-9
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- IntroductionPublished by Springer Nature ,2006
- The lachrymatory factor of the onion: an NMR studyTetrahedron Letters, 1980
- The chemistry of sulfines. 6. Dimer of the onion lachrymatory factor: the first stable 1,2-dithietane derivativeJournal of the American Chemical Society, 1980
- Stabilities of stereoisomeric imine anionsJournal of the American Chemical Society, 1980
- Ozonolysis. The added aldehyde effectThe Journal of Organic Chemistry, 1980
- Theoretical determination of molecular structure and conformation. 6. The Criegee intermediate. Evidence for a stabilization of its syn form by alkyl substituentsJournal of the American Chemical Society, 1979
- Stereochemistry of ozonide formation. Effects of complexing agents and rate of warm-upJournal of the American Chemical Society, 1978
- The stereochemical consequences of electron delocalization in extended .pi. systems. An interpretation of the cis effect exhibited by 1,2-disubstituted ethylenes and related phenomenaJournal of the American Chemical Society, 1976
- The Dependence of Conformational and Isomer Stability on the Number of Electrons in Extended π SystemsJournal of the American Chemical Society, 1966
- Microwave Spectrum of Methyl ThionylamineThe Journal of Chemical Physics, 1965