Synthesis of regio- and stereospecifically C-deuterated derivatives of glycosidase inhibitors 1-deoxymannojirimycin and 2,5-dideoxy-2,5-imino-D-mannitol by intramolecular reductive amination employing deuterium gas

Andreas Berger, Martin Fechter, Günther Gradnig, Christian Mirtl, Werner Schmid, Arnold Stütz

Research output: Contribution to journalArticleResearchpeer-review

Original languageEnglish
Pages (from-to)367-374
JournalCarbohydrate Research
Volume309
Publication statusPublished - 1998

Cite this

Synthesis of regio- and stereospecifically C-deuterated derivatives of glycosidase inhibitors 1-deoxymannojirimycin and 2,5-dideoxy-2,5-imino-D-mannitol by intramolecular reductive amination employing deuterium gas. / Berger, Andreas; Fechter, Martin; Gradnig, Günther; Mirtl, Christian; Schmid, Werner; Stütz, Arnold.

In: Carbohydrate Research, Vol. 309, 1998, p. 367-374.

Research output: Contribution to journalArticleResearchpeer-review

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title = "Synthesis of regio- and stereospecifically C-deuterated derivatives of glycosidase inhibitors 1-deoxymannojirimycin and 2,5-dideoxy-2,5-imino-D-mannitol by intramolecular reductive amination employing deuterium gas",
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journal = "Carbohydrate Research",
issn = "0008-6215",
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T1 - Synthesis of regio- and stereospecifically C-deuterated derivatives of glycosidase inhibitors 1-deoxymannojirimycin and 2,5-dideoxy-2,5-imino-D-mannitol by intramolecular reductive amination employing deuterium gas

AU - Berger, Andreas

AU - Fechter, Martin

AU - Gradnig, Günther

AU - Mirtl, Christian

AU - Schmid, Werner

AU - Stütz, Arnold

PY - 1998

Y1 - 1998

M3 - Article

VL - 309

SP - 367

EP - 374

JO - Carbohydrate Research

JF - Carbohydrate Research

SN - 0008-6215

ER -