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Published in 2022 at "Organic letters"
DOI: 10.1021/acs.orglett.2c01561
Abstract: A general and diastereoselective fluorination/glycosylation strategy for the synthesis of 2'-fluorinated nucleosides has been developed. Electrophilic fluorination of a glycal with NFSI provided the 1',2'-difunctionalized furanoside intermediate with high diastereoselectivity. The TBS-protected 2'-deoxyfluorosulfonimide sugar was…
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Keywords:
deoxy fluoronucleosides;
diastereoselective method;
syn deoxy;
construction syn ... See more keywords