Syntheses and absolute configurations of the marine sponge purines (+)-agelasimine-A and (+)-agelasimine-B

Add time:08/28/2019    Source:sciencedirect.com

The first total syntheses of (+)-agelasimine-A and (+)-agelasimine-B, adenine-related bicyclic diterpenoids isolated from the marine sponge Agelas mauritiana, have been achieved via a highly stereoselective route. On the basis of the present results, the absolute configurations of both alkaloids have been defined as shown in stereoformulas (+)-1a and (+)-1b, respectively.

We also recommend Trading Suppliers and Manufacturers of agelasimine A (cas 114216-85-2). Pls Click Website Link as below: cas 114216-85-2 suppliers

Prev:3-(Aminomethyl)piperazine-2,5-dione as a novel NMDA glycine site inhibitor from the chemical universe database GDB
Next:Racemic syntheses of agelasimine-A and agelasimine-B, bicyclic diterpenoids from the marine sponge Agelas mauritiana)