메뉴 건너뛰기




Volumn 37, Issue 42, 1996, Pages 7645-7648

Building blocks for glycopeptide synthesis: Preparation of α-O-fucosylated Fmoc serine and threonine in one step from L-fucose tetraacetate

Author keywords

[No Author keywords available]

Indexed keywords

GLYCOPEPTIDE;

EID: 0030583470     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(96)01702-9     Document Type: Article
Times cited : (22)

References (16)
  • 2
    • 0002490637 scopus 로고
    • Glycopeptide synthesis
    • Lee, Y. C.; Lee, R. T. Eds.; Academic Press, Inc.: San Diego
    • 2. Meldal, M. Glycopeptide synthesis. In Neoglycoconjugates: Preparation and Applications; Lee, Y. C.; Lee, R. T. Eds.; Academic Press, Inc.: San Diego, 1994; pp. 145-198.
    • (1994) Neoglycoconjugates: Preparation and Applications , pp. 145-198
    • Meldal, M.1
  • 15
    • 85030271629 scopus 로고    scopus 로고
    • 1,2,3,4-Tetra-O-acetyl-L-fucopyranose (1) was obtained as an anomeric mixture (α:β, 10:1) by acetylation of L-fucose with acetic anhydride in pyridine. The anomeric mixture of 1 was used as glycosyl donor after purification by flash column chromatography
    • 15. 1,2,3,4-Tetra-O-acetyl-L-fucopyranose (1) was obtained as an anomeric mixture (α:β, 10:1) by acetylation of L-fucose with acetic anhydride in pyridine. The anomeric mixture of 1 was used as glycosyl donor after purification by flash column chromatography.
  • 16
    • 85030274733 scopus 로고    scopus 로고
    • note
    • 3). NMR data were in agreement with those published in ref. 12.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.