Publication details
Stereoselective 1,3-Dipolar Cycloaddition Reactions of gamma-Substituted alpha-Methylene-gamma-lactones
| Authors | |
|---|---|
| Year of publication | 2000 |
| Type | Article in Proceedings |
| Conference | 8th Blue Danube Symposium on Heterocyclic Chemistry, Program, Abstract of Papers, List of Participants |
| MU Faculty or unit | |
| Citation | |
| Field | Organic chemistry |
| Description | Diatereoselectivity of 1,3-dipolar cycloaddition reactions to alpha-methylene-gamma-lactone dipolaropholes was controlled by placing a bulky substituent (OBO) into gamma-position of lactone ring. The enantiomerically pure dipolarophiles were prepared in good yield from easy accessible L-glutamic acid. |
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