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Chemo-enzymatic Synthesis of N-glycans for Array Development and HIV Antibody Profiling
Published on: February 5, 2018
Noteworthy observations accompanying synthesis of the apoptolidin disaccharide
Madduri Srinivasarao1, Taesik Park, Yuzhong Chen
1Department of Chemistry, Purdue University, West Lafayette, Indiana 47907, USA.
Abstract:
A stereoselective synthesis of the apoptolidin disaccharide is reported. The key chemistry features a new transformation utilizing a highly selective tetramethylalkoxyalanate[v]-directed syn-methylation of a vinylogous ester, isolation of a hydrate of a 2-keto sugar, an eco-friendly radical cleavage of a bromomethyl group, and an efficient preparation of a fluorodisaccharide via the use of XtalFluor-E.
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