An all-cis 3,4-dihydroxy-5-aminopiperidine by a novel route to deoxydiamino sugars

Tetrahedron Letters

Volumn 40, Issue 11, 1999, Pages 2099-2100

  Swaleh, Sauda ^a   Liebscher, Jürgen ^a  

^a HUMBOLDT UNIVERSITY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

3,4 DIHYDROXY 5 AMINOPIPERIDINE; DIAMINO ACID; PIPERIDINE DERIVATIVE; UNCLASSIFIED DRUG;

ALKYLATION; ARTICLE; CATALYSIS; CHIRALITY; DERIVATIZATION; DRUG SYNTHESIS; ENANTIOMER; HYDROGENATION; HYDROLYSIS;

EID: 0033548456     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)00156-2     Document Type: Article

References (7)

1. Ferrier, R.J.; Blattner, R.; Clinch, K., Fumeaux, R.H.; Gadiner, J.M.; Tyler, P.C.; Wightman, R.H.; Williams, N.R. A Specialist Periodical Report, The Royal Society of Chemistry in Carbohydrate Chemistry 1996, 28, 120.
2. Herdeis, C.; Schiffer, T. Tetrahedron 1996, 52, 14745 and references cited therein.
3. Kiciak, K.; Jacobsson, U.; Golebiowski, A.; Jurczak, J. Polish J. Chem. 1994, 68, 199 and references cited therein.
4. Faltz, H.; Radspieler, A.; Liebscher, J. Synlett 1997, 1071.
5. Boyd, G.V. in Comprehensive Heterocyclic Chemistry (ed. Katritzky, A. R.; Rees, C. W.) 1984, Vol. 6, p. 177.
6. Ott, D.G.; Hayes, F.N.; Kerr, V.N. J. Amer.Chem.Soc., 1956, 78, 1941.
7. 3). The relative configuration was confirmed by X-ray crystal analysis of racemic 7 obtained from racemic rather than from enantiopure 3. Full details of the structure determination of racemic have been deposited at the Fachinformationszentrum Karlsruhe, Gesellschaft für Wissenschaftlich-technische Information mbH, D-76344 Eggenstein-Leopoldshafen, Germany. A full literature citation and the reference number CSD 410369 should be quoted for any request of the material.