Cyanopivaloyl Ester in the Automated Solid-Phase Synthesis of Oligorhamnans.

ABSTRACT: The development of effective protecting group chemistry is an important driving force behind the progress in the synthesis of complex oligosaccharides. Automated solid-phase synthesis is an attractive technique for the rapid assembly of oligosaccharides, built up of repetitive elements. The fact that (harsh) reagents are used in excess in multiple reaction cycles makes this technique extra demanding on the protecting groups used. Here, the synthesis of a set of oligorhamnan fragments is reported using the cyanopivaloyl (PivCN) ester to ensure effective neighboring group participation during the glycosylation events. The PivCN group combines the favorable characteristics of the parent pivaloyl (Piv) ester, stability, minimal migratory aptitude, minimal orthoester formation, while it can be

SUBMITTER: Geert Volbeda A 

PROVIDER: S-EPMC5735374 | biostudies-literature | 2017 Dec

REPOSITORIES: biostudies-literature