Journal
TETRAHEDRON
Volume 56, Issue 4, Pages 639-644Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/S0040-4020(99)01028-5
Keywords
cycloadditions; pyrrolidines; nitro compounds
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We have studied the behaviour of 2-acetoxy-nitroethane derivatives in the presence of triethylamine and of an azomethine ylide generated also by the action of this base in the same reaction mixture. Under these conditions the nitro-olefins are generated and react in situ with the corresponding dipoles, giving pyrrolidine derivatives in moderate to good yields. (C) 2000 Elsevier Science Ltd. All rights reserved.
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