Quantum chemical study of tautomerism of bullvalene, bullvalenol, and the corresponding ketone

[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 .