Abstract
The 1,3-dipolar cycloaddition of acrylates derived from 9-anthrylcarbinol to a cyclic nitrone is studied. The composition of the reaction product depends on the steric hindrance of the substituent. A complete study of the diastereoisomers was performed by NMR and we were thus able to determine the absolute configuration of the major adducts.
Original language | English |
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Pages (from-to) | 2793-2796 |
Journal | Tetrahedron Asymmetry |
Volume | 7 |
Issue number | 10 |
DOIs | |
Publication status | Published - 1 Jan 1996 |