1,5-versus 1,3-Dipolar reactivity of azomethine imines
Abstract
The azomethine imines (1) function as 6π-electron 1,5-dipoles rather than 4π-electron 1,3-dipoles in their cycloaddition to acetylenedicarboxylic esters.
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J. Chem. Soc., Chem. Commun., 1972, 806-807
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1,5-versus 1,3-Dipolar reactivity of azomethine imines
S. F. Gait, M. J. Rance, C. W. Rees and R. C. Storr, J. Chem. Soc., Chem. Commun., 1972, 806 DOI: 10.1039/C39720000806
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