Preferred syn‐Elimination from trans‐1,2‐Dichloro‐ and trans‐1,2‐Dibromocyclodecane
- 22 December 1971
- journal article
- research article
- Published by Wiley in Angewandte Chemie International Edition in English
- Vol. 10 (12), 926-927
- https://doi.org/10.1002/anie.197109261
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Reactions of phosphorus azides with activated alkynesThe Journal of Organic Chemistry, 1970
- Reaction of Trichloramine with Olefins. A Convenient Synthesis of vic-Dichlorides.Synthesis, 1969
- Stereochemical studies. LIV. trans-1,2-Dibromocyclodecane: The synthesis of an elusive compoundCollection of Czechoslovak Chemical Communications, 1969
- Stereochemical studies. LIII. Steric course of cycloalkyl 'onium base eliminations: Direct evidence for the syn-anti elimination dichotomy using deuterium labelled cyclodecyl derivativesCollection of Czechoslovak Chemical Communications, 1968
- Stereochemical studies. L. The mechanism of bimolecular elimination of cycloalkyl tosylates. The scope of syn-elimination: Dependence on reaction conditions and substrate structureCollection of Czechoslovak Chemical Communications, 1968
- Stereochemical studies. IL. The mechanism of cycloalkene formation from cycloalkyl bromides. The scope of the syn-anti bimolecular elimination dichotomyCollection of Czechoslovak Chemical Communications, 1968
- Many-Membered Carbon Rings. V. Cyclodecyne, cis- and trans-Cyclodecene and Related Compounds1Journal of the American Chemical Society, 1952