Journal of the Chemical Society. Chemical communications p. 31 - 32 (1983)
Update date:2022-09-26
Topics:
Beugelmans, R.
Negron, G.
Roussi, G.
The first azomethine ylide devoid of a stabilizing group, generated by treating trimethylamine N-oxide with lithium di-isopropylamide, undergoes a ready <3 + 2> cycloaddition with various simple alkenes to give high yields of the corresponding pyrrolidine
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