Abstract
An efficient route to two 3- O-acyl-2-deoxy-4,6- O-isopropylidene-2-trichloroacetamido- d-glucopyranosyl trichloroacetimidate donors is reported. As demonstrated for the 3- O-acetyl derivative, these building blocks are exquisite β- d-glucosamine donors when reacted either with simple alcohols or with complex oligosaccharides. Besides, their protection pattern is compatible with selective deprotection and subsequent chain elongation at O-3 of the newly incorporated glucosamine residue.
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.
