Asymmetric cyclopentannulation reactions: scope and limitation
The first part of this dissertation is devoted to the study of an asymmetric [3+2] cycloaddition sequence developed in our laboratory. The cycloaddition sequence used a sulfonamide-based homoenolate equivalent which was cyclocondensed with a cyclic enone. The stereochemistry of the final product was...
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| Format: | Others |
| Language: | en |
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Universite catholique de Louvain
2003
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| Online Access: | http://edoc.bib.ucl.ac.be:81/ETD-db/collection/available/BelnUcetd-09242003-153934/ |