Castanospermine

A naturally occurring alkaloid with potential medicinal applications.

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The synthesis of ester and ketone analogues of 1-deoxynojirimycin and castanospermine
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Enantiospecific synthesis of polyhydroxylated indolizidines related to castanospermine: (6R, 7S, 8aR) - 6,7-dihydroxyindolizidine and (6R, 7R, 8S, 8aR) - 6,7,8-trihydroxyindolizidine
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- OCTAHYDRO-INDOLIZINE-6,7-DIOL
TOTAL SYNTHESES OF (+)-CASTANOSPERMINE AND (+)-DEOXYNOJIRIMYCIN
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- (3S,4S,5S,6S)-3,4,5,6-TETRAHYDROXYAZEPANE HCL
Cycloaddition Reactions of Carbohydrate Derivatives. Part VI. Quinolizidine Analogs of Castanospermine
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- N-benzyl-(6R,1'S,2'R,3'R,4'R)-6-(3'-O-benzyl-1',2':5',6'-di-O-isopropylidene-1',2',3',4',5'-pentahydroxy-1'-pentyl)-2,3-didehydropiperidine-4-one
Asymmetric synthesis of 1-deoxy-8,8a-di-epi-castanospermine
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- [(4S,5S)-5-((2S,3S,6S)-3-Azido-6-methoxy-tetrahydro-pyran-2-yl)-2,2-dimethyl-[1,3]dioxolan-4-ylmethoxy]-tert-butyl-diphenyl-silane

Synthesis Asymmetric synthesis Flash chromatography Column chromatography Ester NMR spectroscopy Recrystallization Catalytic hydrogenation Total synthesis Mass spectrometry (MS) Enantioselective synthesis Ketone Optical rotation High-performance liquid chromatography (HPLC) TLC (thin-layer chromatography) Protecting group Analogues Cycloaddition Reactions Reductive Amination Enantiospecific Chiral Auxiliary Characterization Techniques Ring-Closing Metathesis Experimental conditions Polyhydroxylated Indolizidines 1-Deoxynojirimycin Indolizidine Chiral reagents Carbohydrate Derivatives Glycosidase Inhibitor

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