Abstract
AbstractProton and carbon chemical shift data and proton–proton coupling constants of the synthetic antithrombotic pentasaccharide SanOrg34006 and its synthetic precursors are reported. Long‐range heteronuclear correlation experiments allow the determination of the substitution pattern of the protecting groups in the precursor molecules. Also, the sequence of the oligosaccharide was confirmed this way. The conformation of the α‐L‐iduronic acid moiety was studied by the analysis of the 3J(1H,1H) coupling constants. Copyright © 2001 John Wiley & Sons, Ltd.
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
