| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5248460 | Tetrahedron | 2013 | 8 Pages |
Abstract
The reactions of norbornene, norbornadiene and 7-oxanorbornene with methyl 3-(chloromethyl) phenoxyacetate (4), optically pure (S)-1-octyn-3-ol (5), and 8% Pd(PPh3)4 afford in one step satisfactory yields of the corresponding esters 6, 7 and 8 respectively, readily saponified to the first interphenylene prostaglandin endoperoxide analogs 10, 11 and 12 respectively.
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Authors
Richard C. Larock, Srinivasan Babu,