| Literature DB >> 29249147 |
Yuta Maki1, Takanori Mima1, Ryo Okamoto1, Masayuki Izumi1, Yasuhiro Kajihara1.
Abstract
Poly-N-acetyllactosamine (poly-LacNAc) structures on glycoproteins play important roles in essential biological events such as cell-cell adhesion. Here, we report a new strategy for the semisynthesis of LacNAc-extended complex-type biantennary oligosaccharides. We found an efficient isopropylidenation reaction that selectively protects the terminal Gal-3,4-OH of a biantennary complex-type nonasaccharide isolated from a natural source. This finding enabled the conversion of the nonasaccharide into the two types of oligosaccharides containing di-LacNAc units at one or two antennae via ten-step chemical sequences.Entities:
Year: 2017 PMID: 29249147 DOI: 10.1021/acs.joc.7b02485
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354