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Synthesis of O-linked Carbasugar Analogues of Galactofuranosides and N-linked Neodisaccharides

Frigell, Jens, 1979- (author)
Stockholms universitet,Institutionen för organisk kemi,Ian Cumpstey
Cumpstey, Ian, Dr (thesis advisor)
Centre National de la Recherche Scientifique, Institut de Chimie des Substances Naturelles
Fleet, George, Professor (opponent)
Oxford University, Department of Chemistry
 (creator_code:org_t)
ISBN 9789174471687
Stockholm : Department of Organic Chemistry, Stockholm University, 2010
English 80 s.
  • Doctoral thesis (other academic/artistic)
Abstract Subject headings
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  • In this thesis, carbohydrate mimicry is investigated through the syntheses of carbohydrate analogues and evaluation of their inhibitory effects on carbohydrate-processing enzymes. Galactofuranosides are interesting structures because they are common motifs in pathogenic microorganisms but not found in mammals. M.tuberculosis, responsible for the disease tuberculosis, has a cell wall containing a repeating unit of alternating (1→5)- and (1→6)-linked β-D-galactofuranosyl residues. Synthetic inhibitors of the enzymes involved in the biosynthesis of the cell wall could find great therapeutic use. The first part of this thesis describes the first synthesis of the hydrolytically stable carbasugar analogue of galactofuranose, 4a-carba-β-D-Galf, and the synthetic work of synthesising β-linked pseudodisaccharides containing carba-Galf, which were tested for glycosyltransferease inhibitory activity. The pseudodisaccharide carba-Galf-(β1→5)-carba-Galf was found to be a moderate inhibitor of the glycosyltransferase GlfT2 of M.tuberculosis. The thesis also describes how a general method towards biologically relevant α-linked carba-Galf ethers was developed. The final part of this thesis is focussed on the formation of nitrogen-linked monosaccharides without the participation of the anomeric centre. Such a mode of coupling is called tail-to-tail neodisaccharide formation. The couplings of carbohydrate derivatives via the Mitsunobu reaction are successfully reported herein. The method describes the key introduction of an allylic alcohol in the electrophile and the subsequent functionalisation of the alkene to obtain the neodisaccharide. Two synthesised neodisaccharides presented in this thesis have been sent to be tested for glycosidase inhibitory activity.

Subject headings

NATURVETENSKAP  -- Kemi -- Organisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Organic Chemistry (hsv//eng)

Keyword

carbasugar
galactofuranose
mycobacterium
tuberculosis
ring-closing metathesis
GlfT2
galactan
epoxide-opening
pseudodisaccharide
etherification
regioselective
carbohydrate
carbocycles
glycomimetics
glucosidase
neodisaccharides
Mitsunobu
Organic synthesis
Organisk syntes
organisk kemi
Organic Chemistry

Publication and Content Type

vet (subject category)
dok (subject category)

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