Synthesis of the C1-C9 segment of epothilons
- authored by
- Eckhard Claus, Axel Pahl, Peter G. Jones, Hartmut M. Meyer, Markus Kalesse
- Abstract
The C1-C9 segment of epothilons was generated by an aldol reaction between chiral aldehyde 3 and ethyl ketone 4. Removal of the TBS protecting groups and debenzylation generated spiro ketal 13 which was analyzed by X-ray crystallography.
- External Organisation(s)
-
Technische Universität Braunschweig
- Type
- Article
- Journal
- Tetrahedron letters
- Volume
- 38
- Pages
- 1359-1362
- No. of pages
- 4
- ISSN
- 0040-4039
- Publication date
- 24.02.1997
- Publication status
- Published
- Peer reviewed
- Yes
- ASJC Scopus subject areas
- Biochemistry, Drug Discovery, Organic Chemistry
- Electronic version(s)
-
https://doi.org/10.1016/S0040-4039(96)02493-8 (Access:
Unknown)