Abstract
Methyl α-isomaltoside and methyl α-isomaltotrioside specifically deoxygenated at position C-3 of various glucopyranosyl units were synthesized by condensation of either 1,6- di-O- acetyl-2,4-di-O- benzyl-3-deoxy-α,β- d -ribo- hexopyranose (7) or 1,6- di-O- acetyl-2,3,4-tri-O- benzyl-α,β- d-glucopyranose [mediated by silver perchlorate and tin(IV) chloride] with suitably blocked derivatives of methyl α- d-glucopyranoside, its 3-deoxy analog (6), or methyl 3′-deoxy α-isomaltoside (10), respectively.
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.
