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1.
Carbohydr Res ; 341(7): 846-54, 2006 May 22.
Article in English | MEDLINE | ID: mdl-16529731

ABSTRACT

The synthesis of 2(R),3-dihydroxypropyl and 2(R),3(R)-dihydroxybutyl beta-d-fructopyranosides, and some derivatives, employing Sharpless-type catalytic asymmetric dihydroxylation procedures is described. Some aspects of the reactions, including stereoselectivities and chemical evidence for the assigned stereochemistry of the main products are reported.


Subject(s)
Aminoglycosides/chemical synthesis , Aminoglycosides/chemistry , Catalysis , Hydroxylation , Molecular Conformation , Molecular Structure , Stereoisomerism , Temperature
2.
Bioorg Med Chem ; 13(1): 223-36, 2005 Jan 03.
Article in English | MEDLINE | ID: mdl-15582467

ABSTRACT

A series of cycloalkyl-substituted oxo-alkanedicarboxylic acids have been prepared by the TosMIC methodology departing from haloalkyl-substituted cycloalkylcarboxylic esters. cyclopropyl derivatives showed IC(50) activity in the 0.3-1.0 microM range on the de novo incorporation of radiolabeled acetate into lipids in primary cultures of rat hepatocytes, and they showed lipid-regulating properties when tested in vivo in female obese Zucker fatty rats.


Subject(s)
Dicarboxylic Acids/pharmacology , Lipids/blood , Lipoproteins/blood , Animals , Cells, Cultured , Dicarboxylic Acids/chemistry , Hepatocytes/drug effects , Hepatocytes/metabolism , Magnetic Resonance Spectroscopy , Male , Mass Spectrometry , Rats , Rats, Sprague-Dawley
3.
Carbohydr Res ; 337(12): 1083-7, 2002 Jun 12.
Article in English | MEDLINE | ID: mdl-12062523

ABSTRACT

Carbohydrate based syntheses of azasugars with unusual configurations viz. 1,5-dideoxy-1,5-imino-L-gulitol (L-guloDNJ) and 1,5-dideoxy-1,5-imino-L-talitol (L-taloDNJ) are reported, from D-mannose and D-fructose, respectively. The key steps in both syntheses involved reductive aminative cyclizations. Thus, L-guloDNJ was obtained by reduction of 2,3;4,6-di-O-isopropylidene-5-O-p-toluenesulfonyl-D-mannononitrile with LiAlH(4) in DME to give the protected azasugar which upon hydrolysis with HCl afforded crystalline L-guloDNJ as the HCl salt in 29% overall yield. Reduction of 6-azido-1-O-tert-butyldimethylsilyl-2,3-O-isopropylidene-beta-D-ribohexulofuranose obtained from D-fructose in six steps, followed by treatment with HCl, afforded L-taloDNJ as an HCl salt in approximately 10% overall yield.


Subject(s)
1-Deoxynojirimycin/analogs & derivatives , 1-Deoxynojirimycin/chemical synthesis , 1-Deoxynojirimycin/chemistry , Molecular Structure , Stereoisomerism
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