Iminosugars from α,β-epoxyamides. Part 2: Synthetic approach to hydroxylated pyrrolidine and azepane derivatives

Tetrahedron Letters

Volumn 45, Issue 12, 2004, Pages 2611-2613

  Assiego, C ^a   Pino Gonzalez M S ^a   Lopez Herrera F J ^a  

^a UNIVERSITY OF MÁLAGA   (Spain)

Author keywords

Azasugar; Azepane; Epoxide opening; Epoxyamide; Homoiminosugar; Pyrrolidine

Indexed keywords

AMIDE; AZEPINE DERIVATIVE; CARBOHYDRATE; EPOXIDE; IMINOSUGAR DERIVATIVE; PIPERIDINE DERIVATIVE; PYRROLIDINE DERIVATIVE; RIBOSE; UNCLASSIFIED DRUG;

ARTICLE; CHIRALITY; DRUG SYNTHESIS; HYDROXYLATION;

EID: 1542272307     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.01.144     Document Type: Article

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19. 3): δ 79.5 (C-5), 78.8 (C-4), 69.2 (C-2), 65.7 (C-3), 65.1 (C-6).
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22. Yields are given after product purification and are not optimised. The deprotection of the products is under way in our laboratory and will be reported in a full account of our work.