Quantum chemical study of tautomerism of bullvalene, bullvalenol, and the corresponding ketone
暂无分享,去创建一个
[1] S. G. Semenov,et al. Tautomers of 4,5-dihydroxy-1,8-bis(dimethylamino)naphthalene and related boron compounds: A quantum-chemical study , 2012, Russian Journal of General Chemistry.
[2] Ernest R. Davidson,et al. The Cope rearrangement in theoretical retrospect , 2001 .
[3] Ernest R. Davidson,et al. Diradical Character of the Cope Rearrangement Transition State , 2000 .
[4] S. Alexander,et al. Theory of dynamic magic angle spinning nuclear magnetic resonance and its application to carbon‐13 in solid bullvalene , 1993 .
[5] L. A. Paquette. Stereokontrollierte Synthese komplizierter cyclischer Ketone durch Oxy‐Cope‐Umlagerung , 1990 .
[6] B. Meier,et al. Fluxional behavior in the solid state: bullvalene , 1985 .
[7] J. V. Nelson,et al. A general approach to the synthesis of 1,6-dicarbonyl substrates. New applications of base-accelerated oxy-Cope rearrangements , 1978 .
[8] D. Evans,et al. [3,3]Sigmatropic rearrangements of 1,5-diene alkoxides. Powerful accelerating effects of the alkoxide substituent , 1975 .
[9] J. Barltrop,et al. Excited states in organic chemistry , 1975 .
[10] I. Paul,et al. Crystal structure of bullvalene at 25.degree. , 1967 .
[11] G. Schröder,et al. Neues aus der Bullvalen‐Chemie , 1967 .
[12] Gerhard Schröder,et al. Moleküle mit schneller und reversibler Valenzisomerisierung. (Moleküle mit fluktuierenden Bindungen) , 1965 .
[13] H. S. Gutowsky,et al. Spin-Echo Nuclear Magnetic Resonance Studies of Chemical Exchange. VI. Rearrangment of Bullvalene and of Its Silver Nitrate Complex1 , 1965 .
[14] G. Schröder,et al. Die temperaturabhängigen NMR‐Spektren von Tricyclo[3.3.2.04.6]decadien‐(2.7), einigen seiner Derivate und von Tricyclo[3.3.2.04.6]decatrien‐ (2.7.9) (Bullvalen) , 1964 .
[15] G. Schröder,et al. Moleküle mit schneller und reversibler valenzisomerisierung.II: Synthese und eigenschaften von brombullvalen und tert-butyl-bullvalyläther , 1964 .
[16] Gerhard Schröder,et al. Synthese und Eigenschaften von Tricyclo[3.3.2.04.6]deca‐2.7.9‐trien (Bullvalen) , 1963 .
[17] M. Saunders. Measurement of the rate of rearrangement of bullvalene , 1963 .
[18] H. Zimmerman,et al. BICYCLO[2,2,2]-2,5,7-OCTATRIENE (BARRELENE), A UNIQUE CYCLIC SIX ELECTRON PI SYSTEM , 1960 .
[19] Arthur C. Cope,et al. The Introduction of Substituted Vinyl Groups. V. A Rearrangement Involving the Migration of an Allyl Group in a Three-Carbon System1 , 1940 .