Abstract
The reaction of oxazaphospholanes with acid chlorides of trivalent phosphorus takes place with the cleavage of exo- or endocyclic P-N bonds. The opening of the ring produces diphosphorylated alkanolamines, which are converted as a result of disproportionation into 1,3,2-diheterophospholanes, the latter being products of the exchange of exocyclic substituents.
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 callMore From: Bulletin of the Academy of Sciences of the USSR, Division of chemical science
Paper Title
Journal
Date
