“Tied-back” carbocyclic intermediates in the preparation of very sterically strained olefins: Derivatives of tetra-tert-butylethylene
- 31 December 1981
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 22 (46) , 4563-4566
- https://doi.org/10.1016/s0040-4039(01)82982-8
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Sterisch gehinderte Olefine, VII. Dehydratisierung von aliphatischen Di‐tert‐butylalkylcarbinolen. Kraftfeld‐Rechnungen von sterisch gehinderten EthylenenEuropean Journal of Inorganic Chemistry, 1980
- Multiple extrusion methods for the preparation of sterically hindered olefins. An approach to tetra-tert-butylethyleneThe Journal of Organic Chemistry, 1980
- The introduction of alkylidene substituents into the 4-position of the 3,3,5,5-tetramethyl-Δ1-pyrazoline nucleus by the thioketone plus diazoalkane reaction: synthesis of tetrasubstituted episulphides and alkenesJournal of the Chemical Society, Perkin Transactions 1, 1979
- Rapid chromatographic technique for preparative separations with moderate resolutionThe Journal of Organic Chemistry, 1978
- TetraneopentylethyleneThe Journal of Organic Chemistry, 1977
- A survey of strained organic moleculesChemical Reviews, 1976
- Olefin synthesis by two-fold extrusion processes. Part 3. Synthesis and properties of hindered selenoketones (selones)Journal of the Chemical Society, Perkin Transactions 1, 1976
- Olefin synthesis by two-fold extrusion processes. Part II. Synthesis of some very hindered olefinsJournal of the Chemical Society, Perkin Transactions 1, 1974
- Steric crowding in organic chemistry. VI. Reactivity of tri-tert-butylethylene and related compoundsThe Journal of Organic Chemistry, 1972
- The oxidation of cyclobutanols and aromatic rings with ruthenium tetroxideTetrahedron Letters, 1967