| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5217119 | Tetrahedron | 2013 | 9 Pages |
Abstract
The total syntheses of penmacric acid and its three stereoisomers were accomplished through the intermolecular radical addition reaction of the 4-pyrrolidyl radical derived from trans-4-hydroxy-l-proline. Furthermore, 1â²,3-diepi-penmacric acid was synthesized stereoselectively via double stereoinduction in the radical reaction.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Masafumi Ueda, Ayako Ono, Dai Nakao, Kenji Matsuno, Takeaki Naito, Okiko Miyata,