Letters in Drug Design & Discovery

G. Perry
University of Texas
San Antonio, TX
USA
Email: lddd@benthamscience.org

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Solid-Phase Synthesis of Di-N-Acetyl-β-Chitobiosyl NAG-Thiazoline

Author(s): Gangliang Huang, Ya Chen.

Abstract:

The solid-phase synthesis of di-N-acetyl-β-chitobiosyl NAG (N-acetyl D-glucosamine)-thiazoline 3 was reported. After the 6-O-benzyl NAG-thiazoline 9, NHCbz trichloroacetimidate donors 14, and 21 were synthesized, and solid-phase synthesis was performed using the Wang resin as support. The target di-N-acetyl-β-chitobiosyl NAGthiazoline 3 was obtained by iterative glycosylation reactions, catalytic hydrogenation, acetylation, and deacetylation, respectively.

Keywords: Di-N-acetyl-β-chitobiosyl NAG-thiazoline, Allosamidin analogue, Solid-phase synthesis, Trichloroacetimidate donors, Wang resin, Glycosylation reactions, chitinase, pseudodisaccharide, Streptomyces, thiazoline triacetate 6, Acetylation, TBDMS group, Wang-chlorinated resin, trichloroacetimidate, TMSOTf-promoted glycosylation

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Article Details

VOLUME: 8
ISSUE: 7
Year: 2011
Page: [649 - 651]
Pages: 3
DOI: 10.2174/157018011796235220
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