Regioselective Intramolecular Ring Closure of 2-Amino-6-bromo-2,6-dideoxyhexono-1,4-lactones to 5- or 6-Membered Iminuronic Acid Analogues: Synthesis of 1-Deoxymannojirimycin and of 2,5-Dideoxy-2,5-imino-D-glucitol"

Birgitte M. Malle; Inge Lundt; Tanja Wrodnigg

doi:10.1039/b719631h

Regioselective Intramolecular Ring Closure of 2-Amino-6-bromo-2,6-dideoxyhexono-1,4-lactones to 5- or 6-Membered Iminuronic Acid Analogues: Synthesis of 1-Deoxymannojirimycin and of 2,5-Dideoxy-2,5-imino-D-glucitol"

Birgitte M. Malle, Inge Lundt, Tanja Wrodnigg

Institute of Organic Chemistry (6410)

Research output: Contribution to journal › Article › peer-review

Original language	English
Pages (from-to)	1779-1786
Journal	Organic & Biomolecular Chemistry
Volume	6
DOIs	https://doi.org/10.1039/b719631h
Publication status	Published - 2008

Treatment code (Nähere Zuordnung)

Basic - Fundamental (Grundlagenforschung)

Access to Document

10.1039/b719631h

Cite this

Regioselective Intramolecular Ring Closure of 2-Amino-6-bromo-2,6-dideoxyhexono-1,4-lactones to 5- or 6-Membered Iminuronic Acid Analogues: Synthesis of 1-Deoxymannojirimycin and of 2,5-Dideoxy-2,5-imino-D-glucitol". / Malle, Birgitte M.; Lundt, Inge; Wrodnigg, Tanja.
In: Organic & Biomolecular Chemistry, Vol. 6, 2008, p. 1779-1786.

Research output: Contribution to journal › Article › peer-review

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title = "Regioselective Intramolecular Ring Closure of 2-Amino-6-bromo-2,6-dideoxyhexono-1,4-lactones to 5- or 6-Membered Iminuronic Acid Analogues: Synthesis of 1-Deoxymannojirimycin and of 2,5-Dideoxy-2,5-imino-D-glucitol{"}",

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AU - Lundt, Inge

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