Tetrahedron Letters p. 1191 - 1194 (1990)
Update date:2022-07-31
Topics: Regioselectivity Yield Catalyst Nucleophilic substitution Dipolarophile Alkyl halide Oxime Leaving group Intramolecular Reaction Reaction Mechanism Solvent Effects Stereoselectivity Cycloaddition Tandem Reaction Reaction Optimization 1,3-Dipolar Cycloaddition Heterocycle Intermolecular reaction
Grigg, Ronald
Markandu, Jasothara
Surendrakumar, Sivagnanasundram
Inter-or intra-molecular N-alkylation of oximes or their alkali metal salts furnishes nitrones which can be trapped by activated and non-activated dipolarophiles in inter- and intra-molecular cycloaddition reactions in good yield.
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