Abstract
The action of thionyl chloride on γ -ketoacids was revisited. The reaction does not yield the corresponding γ-ketoacyl chlorides as reported earlier, but instead efficiently produces γ -chlorobutyrolactones. The chemical properties of this function are summarily explored, along with some characteristic spectroscopic data.
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
