Abstract
Abstract In the presence of trityl perchlorate, 1-O-bromoacetyl-β-d-glucose stereoselectively reacts with alcohols to give the corresponding α-glucosides in good yields. The similar reaction of 1-O-acetyl-β-d-ribose affords the corresponding β-ribosides exclusively, while in the presence of molecular sieves 4A and lithium perchlorate, α-ribosides are prepared predominantly in good yields.
Sign-in/Register to access full text options 
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 callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
