Abstract
Michael addition products of secondary allylamines to nitroalkenes were captured as the O-silyl α-allylaminoalkylnitronates. These undergo stereoselective intramolecular silyl nitronate-olefin 1,3-dipolar cycloaddition to provide highly functionalized pyrrolidines.
Original language | English |
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Pages (from-to) | 3759-3763 |
Number of pages | 5 |
Journal | Journal of Organic Chemistry |
Volume | 60 |
Issue number | 12 |
DOIs | |
State | Published - 1 Jun 1995 |