Homochiral carbon branched piperidines from carbon branched sugar lactones: 4-C-methyl-deoxyfuconojirimycin (DFJ) and its enantiomer - removal of glycosidase inhibition

The value of readily available 2-C-methyl aldonic acids in short syntheses of carbon branched piperidines containing quaternary centers is demonstrated. The effect of the introduction of a 4-C-methyl group into piperidine imino sugar inhibitors of l-fucosidases and d-galactosidases is reported. © 20...

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Main Authors: Hotchkiss, D, Kato, A, Odell, B, Claridge, T, Fleet, G
Format: Journal article
Language:English
Published: 2007
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author Hotchkiss, D
Kato, A
Odell, B
Claridge, T
Fleet, G
author_facet Hotchkiss, D
Kato, A
Odell, B
Claridge, T
Fleet, G
author_sort Hotchkiss, D
collection OXFORD
description The value of readily available 2-C-methyl aldonic acids in short syntheses of carbon branched piperidines containing quaternary centers is demonstrated. The effect of the introduction of a 4-C-methyl group into piperidine imino sugar inhibitors of l-fucosidases and d-galactosidases is reported. © 2007 Elsevier Ltd. All rights reserved.
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spelling oxford-uuid:b2cae2ab-0735-4d03-8aff-411d561bc4012022-03-27T04:14:11ZHomochiral carbon branched piperidines from carbon branched sugar lactones: 4-C-methyl-deoxyfuconojirimycin (DFJ) and its enantiomer - removal of glycosidase inhibitionJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:b2cae2ab-0735-4d03-8aff-411d561bc401EnglishSymplectic Elements at Oxford2007Hotchkiss, DKato, AOdell, BClaridge, TFleet, GThe value of readily available 2-C-methyl aldonic acids in short syntheses of carbon branched piperidines containing quaternary centers is demonstrated. The effect of the introduction of a 4-C-methyl group into piperidine imino sugar inhibitors of l-fucosidases and d-galactosidases is reported. © 2007 Elsevier Ltd. All rights reserved.
spellingShingle Hotchkiss, D
Kato, A
Odell, B
Claridge, T
Fleet, G
Homochiral carbon branched piperidines from carbon branched sugar lactones: 4-C-methyl-deoxyfuconojirimycin (DFJ) and its enantiomer - removal of glycosidase inhibition
title Homochiral carbon branched piperidines from carbon branched sugar lactones: 4-C-methyl-deoxyfuconojirimycin (DFJ) and its enantiomer - removal of glycosidase inhibition
title_full Homochiral carbon branched piperidines from carbon branched sugar lactones: 4-C-methyl-deoxyfuconojirimycin (DFJ) and its enantiomer - removal of glycosidase inhibition
title_fullStr Homochiral carbon branched piperidines from carbon branched sugar lactones: 4-C-methyl-deoxyfuconojirimycin (DFJ) and its enantiomer - removal of glycosidase inhibition
title_full_unstemmed Homochiral carbon branched piperidines from carbon branched sugar lactones: 4-C-methyl-deoxyfuconojirimycin (DFJ) and its enantiomer - removal of glycosidase inhibition
title_short Homochiral carbon branched piperidines from carbon branched sugar lactones: 4-C-methyl-deoxyfuconojirimycin (DFJ) and its enantiomer - removal of glycosidase inhibition
title_sort homochiral carbon branched piperidines from carbon branched sugar lactones 4 c methyl deoxyfuconojirimycin dfj and its enantiomer removal of glycosidase inhibition
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