The C1-C16-segment of lasonolide A has been prepared stereoselectively in high chemical and optical yield starting from 2α-methyl-8-oxabicyclo[3.2.1]oct-6-en-3-one (rac-1).
ChemInform Abstract: Asymmetric Synthesis of the C1—C16 Segment (I) of Lasonolide A.
✍ Scribed by Hartmut Beck; H. Martin R. Hoffmann
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 24 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0931-7597
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✦ Synopsis
Abstract
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📜 SIMILAR VOLUMES
Asymmetric Synthesis of the C(18)-C(24) Unit of Lasonolide A. -The synthesis of the title compound (VIII) proceeds with high chiral efficiency. In six steps, four chiral centers are assembled. A key step is the modified Simpkins-Koga asym. deprotonation of compound (I). The strategy outlined is vers