A formal total synthesis of aklavinone (cas 16234-96-1) via a blocked anthraquinone tautomer
-
Add time:08/06/2019 Source:sciencedirect.com
An advanced intermediate in the Kishi synthesis of aklavinone (cas 16234-96-1) was prepared. Juglone was converted into enone 4. Quinone 6 was then prepared from 4 by Michael addition and elimination of PhSOH and HCN.
We also recommend Trading Suppliers and Manufacturers of aklavinone (cas 16234-96-1). Pls Click Website Link as below: cas 16234-96-1 suppliers
Prev:Enantioselective synthesis of the AB ring system of aklavinone (cas 16234-96-1) via a chemoenzymatic route
Next:A convergent rgiospecific route to the aklavinone (cas 16234-96-1) ring system) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- A convergent rgiospecific route to the aklavinone (cas 16234-96-1) ring system08/07/2019
- Enantioselective synthesis of the AB ring system of aklavinone (cas 16234-96-1) via a chemoenzymatic route08/05/2019
- Chemoenzymatic approach to the AB ring system of aklavinone (cas 16234-96-1)08/04/2019
- Practical asymmetric synthesis of aklavinone (cas 16234-96-1)08/03/2019
- Asymmetric synthesis of the ab-ring of aklavinone (cas 16234-96-1)08/02/2019
- A stereospecific total synthesis of aklavinone (cas 16234-96-1)08/01/2019
- Modification of aklavinone (cas 16234-96-1) and aclacinomycins in vitro and in vivo by rhodomycin biosynthesis gene products07/31/2019
- Structural Basis for Substrate Recognition and Specificity in aklavinone (cas 16234-96-1)-11-Hydroxylase from Rhodomycin Biosynthesis07/30/2019
- Characterization of aklavinone (cas 16234-96-1)-11-hydroxylase from Streptomyces purpurascens07/29/2019
