Abstract
AbstractSince the advent of the armed–disarmed strategy, thioglycosides have become essential tools in one-pot oligosaccharide synthesis. The continuum of glycosyl donor reactivity has since been expanded to include so-called ‘superarmed’ thioglycoside donors whose reactivity relies on more than just the inductive effects of protecting groups. Here we report a new method for the synthesis of superarmed thioglycosides via the ring opening of 1,2-orthoesters. This method ensures the necessary 1,2-trans stereochemistry, and importantly, makes use of trimethylsilyl thioethers as sulfur nucleophiles to avoid the use of unpleasant free thiols. Ten examples of ethyl and phenyl thioglycosides of mono- and disaccharides were synthesised from their orthoesters using tris(pentafluorophenyl)borane (BCF) as the Lewis acid promoter and were obtained in good yield and purity.
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.
