
Tetrahedron p. 4495 - 4518 (1991)
Update date:2022-08-04
Topics: Nitrones Michael addition Tandem Reaction 1,3-Dipolar Cycloaddition Oximes 1,3-dipoles
Armstrong, Paul
Grigg, Ronald
Heaney, Frances
Surendrakumar, Sivagnanasundram
Warnock, William J.
C-3, -4, -5, and -6-Alkenyl oximes react with electronegative olefins at the nitrogen atom via a Michael addition or ene-type process to generate the corresponding C-alkenyl nitrones which undergo an intramolecular cycloaddition.The cycloaddition can occu
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