Abstract
A mild and efficient procedure has been developed for the synthesis of triaryl diethers and has been applied to the synthesis of 1, 2 and 3, degradation products from glycopeptide antibiotics of the vancomycin family
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
