Stereochemistry of the cyclopropyl-allyl rearrangements. : II. Thermal ring opening of the chlorofluorocarbene-norbornene adducts.
- 31 December 1967
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 8 (29) , 2773-2776
- https://doi.org/10.1016/s0040-4039(00)90856-6
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Stereochemical consequences of the reaction of monohalocarbene with norborneneTetrahedron Letters, 1966
- Chemistry of gem-Dihalocyclopropanes. IV. Ring Opening of gem-Dichlorocyclopropyl EthersThe Journal of Organic Chemistry, 1966
- Bridged Polycyclic Compounds. XXXI. Stereochemical Aspects of the Solvolysis of Cyclopropyl Chlorides1Journal of the American Chemical Society, 1965
- The Stereochemistry of the Bicyclo[3.2.1]octane System. III.1,2 The Addition of Dihalocarbene to Bicyclic OlefinsJournal of the American Chemical Society, 1965
- Stereochemistry of Electrocyclic ReactionsJournal of the American Chemical Society, 1965
- sym-Difluorotetrachloroacetone as a Source of ChlorofluorocarbeneThe Journal of Organic Chemistry, 1963