SYNTHESIS OF GLYCOSYLATED AMINO-ACIDS FOR USE IN SOLID-PHASE GLYCOPEPTIDE SYNTHESIS .2. N-(9-FLUORENYLMETHYLOXYCARBONYL)-3-O-[2,4,6-TRI-O-ACETYL-3-O-(2,3,4-TRI-O-ACETYL-ALPHA-D-XYLOPYRANOSYL)-BETA-D-GLUCOPYRANOSYL]-L-SERINE

被引：11

作者：

LUNING, B

NORBERG, T

TEJBRANT, J

机构：

[1] Department of Organic Chemistry, University of Stockholm

来源：

JOURNAL OF CARBOHYDRATE CHEMISTRY | 1992年 / 11卷 / 07期

关键词：

D O I：

10.1080/07328309208018280

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

FMOC-serine phenacylester was glycosylated with a derivative of the disaccharide alpha-D-Xylp-(1 --> 3)-beta-D-Glcp, and the product was treated with zinc to remove the phenacyl group. The title derivative is useful for synthesis of blood clotting factor IX glycopeptide fragments by the solid-phase approach.

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页码：933 / 943

页数：11

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