Synthesis of a taxinine analog via the intramolecular Diels-Alder cycloaddition
-
Add time:08/19/2019 Source:sciencedirect.com
The synthesis of the tricyclic ring system of the taxane diterpenes via an A→ABC intramolecular Diels-Alder construction, and the elaboration of the cycloadduct 13 to taxinine analog 17 are described.
We also recommend Trading Suppliers and Manufacturers of taxinine M (cas 135730-55-1). Pls Click Website Link as below: cas 135730-55-1 suppliers
Prev:Modulation of multidrug resistance in tumor cells by taxinine derivatives
Next:Stereoselective epoxidation of 4(20)-exomethylene in taxinine derivatives and assignment of the epoxide orientation by NMR) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- The NMR spectra of taxinine and its derivatives08/22/2019
- Highly increased cellular accumulation of vincristine, a useful hydrophobic antitumor-drug, in multidrug-resistant solid cancer cells induced by a simply reduced taxinine08/21/2019
- Stereoselective epoxidation of 4(20)-exomethylene in taxinine derivatives and assignment of the epoxide orientation by NMR08/20/2019
- Modulation of multidrug resistance in tumor cells by taxinine derivatives08/18/2019
- Crystal and solution state conformations of two taxoids, taxinine and taxinine B08/17/2019
- Synthesis and antitumor activity of 2-(m-substituted-benzoyl)baccatin III analogs from taxinine08/16/2019


