Di-tert-butylsilylene-directed alpha-selective synthesis of p-nitrophenyl T-antigen analogues

Glycoconj J. 2009 Jan;26(1):83-98. doi: 10.1007/s10719-008-9168-y. Epub 2008 Aug 16.

Abstract

Seven analogues of p-nitrophenyl T-antigen [Galbeta(1-->3)GalNAcalpha(1-->O)PNP] have been synthesized as potential substrates for elucidation of the substrate specificity of endo-alpha-N-acetylgalactosaminidase. These compounds, which are commercially unavailable, include: GlcNAcbeta(1-->3){GlcNAcbeta(1-->6)}GalNAcalpha(1-->O)PNP [core 4 type], GalNAcalpha(1-->3)GalNAcalpha(1-->O)PNP [core 5 type], GlcNAcbeta(1-->6)GalNAcalpha(1-->O)PNP [core 6 type], GalNAcalpha(1-->6)GalNAcalpha(1-->O)PNP [core 7 type], Galalpha(1-->3)GalNAcalpha(1-->O)PNP [core 8 type], Glcbeta(1-->3)GalNAcalpha(1-->O)PNP and GalNAcbeta(1-->3)GalNAcalpha(1-->O)PNP. The assembly of these synthetic probes was accomplished efficiently, based on di-tert-butylsilylene(DTBS)-directed alpha-galactosylation as a key reaction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens / chemistry*
  • Antigens / immunology
  • Butanes / chemistry*
  • Butanes / immunology
  • Nitrophenols / chemical synthesis*
  • Nitrophenols / immunology
  • Silanes / chemistry*
  • Silanes / immunology
  • T-Lymphocytes / immunology*

Substances

  • Antigens
  • Butanes
  • Nitrophenols
  • Silanes
  • di-tert-butylsilylene