Showing papers on "Koenigs–Knorr reaction published in 2017"

TL;DR: Under optimal reaction conditions, both armed and disarmed glycosyl sulfoxide donors were found to react with a range of primary, secondary, and tertiary alcohol acceptors to afford the corresponding glycosides in moderate to good yields with predictable selectivity.

TL;DR: Low temperature NMR revealed that the a-trichloroacetimidate was transformed into the glycosyl fluoride with inversion of stereochemistry, whereas the b-anomer was not.