5-amino-5-deoxy-2-C-hydroxymethyl-2,3-O-isopropylidene-D-talono-1,5-lactam

5-amino-5-deoxy-2-C-hydroxymethyl-2,3-O-isopropylidene-D-talono-1,5-lactam

The title compound, C10H17NO6, was prepared by carrying out three SN2 displacements on a branched sugar derivative, one of which was not planned. Its crystal structure was determined to confirm the identity and stereochemistry of the product. © 2004 International Union of Crystallography Printed in...

Deskribapen osoa

Xehetasun bibliografikoak
Egile Nagusiak:	van Ameijde, J, Cowley, A, Fleet, G, Nash, R, Simone, M, Soengas, R
Formatua:	Journal article
Hizkuntza:	English
Argitaratua:	2004

Antzeko izenburuak

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Synthesis of three branched iminosugars [(3R,4R,5S)-3-(hydroxymethyl)piperidine-3,4,5-triol, (3R,4R,5R)-3-(hydroxymethyl)piperidine-3,4,5-triol and (3S,4R,5R)-3-(hydroxymethyl)piperidine-3.4,5-triol] and a branched trihydroxynipecotic acid [(3R,4R,5R)-3,4,5-trihydroxypiperidine-3-carboxylic acid] from sugar lactones with a carbon substituent at C-2
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Crystal structure of 4-amino-4-deoxy-5,6-O-isopropylidene-D-gulitol, C9H19NO5
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1,2 : 3,4-Di-O-isopropylidene-beta-D-psicofuranose
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1,2 : 3,4-Di-O-isopropylidene-alpha-D-tagatofuranose
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