text.skipToContent text.skipToNavigation

Maximum quantity allowed is 999

请选择数量

p-Methoxyphenylglycosides

A thoughtful choice of anomeric blocking group is often of conclusive importance for the success of an oligosaccharide synthesis. The anomeric blocking group is required stability towards the reaction conditions employed and easy transformation into an activated derivative for further glycosylation.
The p-methoxyphenyl group is useful anomeric blocking group which is removed selectively by treatment with ceric ammonium nitrate, to give the corresponding glycosyl halides and thiophenyl glycosides in high yields. Furthermore, they are stable under most of the conditions used in oligosaccharide synthesis.

References

  • 1) T. Nakano, Y. Ito, T. Ogawa, Tetrahedron Lett. 1990, 31, 1597.
  • 2) M. Mori, Y. Ito, T. Ogawa, Carbohydr. Res. 1989, 192, 131.
  • 3) Y. Matsuzaki, Y. Ito, T. Ogawa, Tetrahedron Lett. 1992, 33, 4025.
  • 4) A. Dan, Y. Ito, T. Ogawa, J. Org. Chem. 1995, 60, 4680.
  • 5) C. Murakata, T. Ogawa, Carbohydr. Res. 1992, 235, 95.
  • 6) H. Kuyama, T. Nukada, Y. Nakahara, T. Ogawa, Tetrahedron Lett. 1993, 34, 2171.
  • 7) Z. Zhang, G. Mugnusson, Carbohydr. Res. 1996, 925, 41.
會話狀態
當前會話將在10分鐘後超時,並返回主頁。請點擊按鈕繼續瀏覽。分鐘後超時,並返回主頁。請點擊按鈕繼續瀏覽。

您的會話已超時,將返回至主頁。

Switching regions will sign you out of your current session. Do you want to continue?