The asymmetric synthesis of the Cl-Cy ferensimycin synthon 3 is described. The absolute stereochemrcal relationships in this target structure were established through chn-al enolate methodology. As part of an ongoing effort to develop asymmetric carbon-carbon bond-forming reactions in the context of
✦ LIBER ✦
Studies directed toward the synthesis of (+)-mycotrienin I. Asymmetric synthesis of the C9N21 aromatic synthon
✍ Scribed by James S. Panek; Michael Yang; Jason Solomon
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- French
- Weight
- 233 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0040-4039
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