Tetrahedron Letters p. 2333 - 2336 (1990)
Update date:2022-09-26
Topics:
Jones, Raymond C. F.
Nichols, John R.
Cox, Michael T.
Azomethine ylides, prepared from imidazolinium salts, undergo 1,3-dipolar cycloaddition with a variety of dipolarophiles to produce hexahydropyrrolo[1,2-α]imidazoles, which are reduced to pyrrolidines; with 2-chloroacrylonitrile as dipolarophile, pyrroles
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