Abstract
Abstract The diastereoselective synthesis of phosphite triesters and their corresponding thiophosphate triesters is described. The new bicyclic imidazo-oxazaphosphorine, synthesized as a single diastereomer, is used as an intermediate that undergoes a diastereoselective displacement when reacted with an alcohol. This process eliminates the use of an acid catalyst.
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Published version (
Free)
Free) 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
