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Synthesis 2009(14): 2403-2407
DOI: 10.1055/s-0029-1216846
DOI: 10.1055/s-0029-1216846
PAPER
© Georg Thieme Verlag
Stuttgart ˙ New York
Synthesis of Functionalized N-Vinyl Nitrogen-Containing Heterocycles
Further Information
Received
2 February 2009
Publication Date:
29 May 2009 (online)
Publication History
Publication Date:
29 May 2009 (online)
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Abstract
Microwave-assisted 1,3-dipolar cycloaddition of the azomethine ylide generated by ring opening of a N-vinylaziridine gave new N-vinyl derivatives of pyrrolidine, 3-pyrroline, octahydropyrrolo[3,4-c]pyrrole and 1,2,4-triazolidine.
Key words
microwave-assisted 1,3-dipolar cycloaddition - Michael addition - allenes - N-vinyl heterocycles - aziridines - pyrrolidines - 3-pyrrolines - octahydropyrrolo[3,4-c]pyrroles - 1,2,4-triazolidines
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