European Journal of Organic Chemistry · 2002 · 29 citations · 21 references
Natural SciencesChemistryGreen ChemistryOrganic ChemistryReaction EngineeringChemical Kinetics ModelingHeterocycle SynthesisHeterocyclic ChemistryOrganic SynthesisReaction MechanismsRetrosynthetic AnalysisOne-pot Heterocycle SynthesisReaction Mechanism DerivationReaction Mechanism ElucidationRing-forming Reactions
1,2,4,5-Tetrazines 7 readily react with 3,3′-bicyclopropenyl 8 in a cycloaddition−cycloelimination sequence to give 3,4-diazanorcaradienes 9 with endo configuration of the methyl group at C-7. On gentle heating in inert solvents, these 3,4-diazanorcaradienes 9 are cleanly transformed into semibullvalenes 11. This reaction sequence can also be performed as a one-pot method. Kinetic investigations and comparisons with two model systems are in agreement with the proposed reaction mechanism.
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A rapidly reversible degenerate cope rearrangement
W. von E. Doering, Wolfgang R. Roth · Tetrahedron · 1963 · 425 citations
A rational synthesis of bullvalene barbaralone and derivatives; bullvalone
W. von E. Doering, B. M. Ferrier, Eric T. Fossel et al. · Tetrahedron · 1967 · 164 citations