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An approach to the synthesis of O-glycopeptides
Stockholm University, Faculty of Science, Department of Organic Chemistry.
1992 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Synthesis of glycopeptides using a solid phase technique has been performed. The preparation of suitably protected glycosylated amino acids and the successful use of these derivatives in solid phase synthesis of two glycopeptides are described. The target molecules were the minimal epitope of the monoclonal antibody FDC6 towards oncofetal human Fibronectin, and a glycosylated cyclic peptide related to the first loop of the EGFlike domain of bovine factor IX.

Place, publisher, year, edition, pages
Stockholm: Stockholm University, 1992. , p. 31
Series
Chemical Communications, ISSN 0366-5607 ; 1992:7
National Category
Organic Chemistry
Identifiers
URN: urn:nbn:se:su:diva-165326Libris ID: 7610810ISBN: 91-7153-064-9 (print)OAI: oai:DiVA.org:su-165326DiVA, id: diva2:1282228
Public defence
1992-12-04, Hörsal G, Arrheniuslaboratorierna, Svante Arrhenius väg 16, Stockholm, 10:00
Note

Härtill 4 uppsatser

Available from: 2019-01-24 Created: 2019-01-24 Last updated: 2019-01-24Bibliographically approved

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CiteExportLink to record
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