ChemInform Abstract: The Total Synthesis of Scytophycin C. Part 1. Stereocontrolled Synthesis of the C1—C32 Protected Seco Acid.
✍ Scribed by I. PATERSON; K.-S. YEUNG; C. WATSON; R. A. WARD; P. A. WALLACE
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 36 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0931-7597
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✦ Synopsis
The Total Synthesis of Scytophycin C. Part 1. Stereocontrolled Synthesis of the C 1 -C 32 Protected Seco Acid.
-A stereocontrolled preparation of the C 1 -C 32 -seco acid ester (XI) required for the total synthesis of the macrolide scytophycin C is presented starting from the aldehyde (S)-(II) in 18% yield and 85% diastereoselectivity. -(
📜 SIMILAR VOLUMES
Studies Directed Toward the Total Synthesis of Scytophycin C: Synthesis of the C 1 -C 18 Fragment of Scytophycin C. -The synthesis of the C-1 to C-18 fragment (X) is based on a highly stereoselective carbon Ferrier-type rearrangement reaction of deoxyglucal (I) and the silyl enol ether (II). -(GRIEC
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