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  SYNTHESIS OF GLYCOSIDES OF FUCOSE UNDER NEUTRAL CONDITIONS IN SOLUTIONS OF LICLO4 IN ORGANIC-SOLVENTS

BOHM, G., & Waldmann, H. (1995). SYNTHESIS OF GLYCOSIDES OF FUCOSE UNDER NEUTRAL CONDITIONS IN SOLUTIONS OF LICLO4 IN ORGANIC-SOLVENTS. TETRAHEDRON LETTERS, 36(22), 3843-3846. doi:10.1016/0040-4039(95)00637-R.

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 Creators:
BOHM, G1, Author
Waldmann, Herbert2, Author           
Affiliations:
1external, ou_persistent22              
2Abt. IV: Chemische Biologie, Max Planck Institute of Molecular Physiology, Max Planck Society, ou_1753290              

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Free keywords: SIALYL-LEWIS-X; OLIGOSACCHARIDES; GLYCOSYLATION; DERIVATIVES; ANTIGENS
 Abstract: The glycosyl donors 2,3,4-tri-0-benzyl fucosyl fluoride and -trichloroacetimidate are activated under neutral conditions in 1M solutions of LiClO4 in CH2Cl2 or ether to react with mono- and disaccharides to give fucosyl glycosides in high yields and with high stereoselectivity.

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Language(s): eng - English
 Dates: 1995
 Publication Status: Issued
 Pages: 4
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Degree: -

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Title: TETRAHEDRON LETTERS
Source Genre: Journal
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Publ. Info: KIDLINGTON, OXFORD : PERGAMON-ELSEVIER SCIENCE
Pages: - Volume / Issue: 36 (22) Sequence Number: - Start / End Page: 3843 - 3846 Identifier: ISSN: 0040-4039