Studies in marine macrolide synthesis: Asymmetric synthesis of C1-C15/C16 subunits of swinholide A and scytophycin C.
-
Add time:08/31/2019 Source:sciencedirect.com
The aldehyde 8, a C1-C15 subunit of swinholide A, was prepared in 10 steps (14.5% yield, 78% ds) by starting with the asymmetric aldol reaction, 15 + 17 → 18. Conversion into the corresponding ethyl ketone 9 provides a C1-C15 subunit of scytophycin C.
We also recommend Trading Suppliers and Manufacturers of swinholide C (cas 132923-51-4). Pls Click Website Link as below: cas 132923-51-4 suppliers
Prev:Brief CommunicationStructural Basis of Swinholide A Binding to Actin
Next:The total synthesis of swinholide A. Part 3: A stereocontrolled synthesis of (−)-pre-swinholide A.) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- The isolation of a monomeric carboxylic acid of swinholide a from the indo-pacific sponge, theonella swinhoei09/04/2019
- The total synthesis of swinholide A. Part 1: A stereocontrolled synthesis of a C19-C32 segment09/03/2019
- The total synthesis of swinholide A. Part 4: Synthesis of swinholide A and isoswinholide A from the protected monomeric seco acid, pre-swinholide A09/02/2019
- The total synthesis of swinholide A. Part 3: A stereocontrolled synthesis of (−)-pre-swinholide A.09/01/2019
- Brief CommunicationStructural Basis of Swinholide A Binding to Actin08/30/2019
- Towards the synthesis of swinholide A and scytophycin C. A highly stereocontrolled synthesis of (−)-pre-swinholide A08/29/2019
- An efficient and stereoselective construction of the C(9)–C(17) dihydropyran segment of swinholides A–C via a novel reductive cleavage of an epoxy aldehyde08/28/2019
- Isoswinholide B and swinholide K, potently cytotoxic dimeric macrolides from Theonella swinhoei08/27/2019
