Studies on Nitro Sugars. VI. Synthesis of Methyl 2-Deoxy-2-nitro-α-D-glucopyranoside Derivatives
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概要
- 論文の詳細を見る
Oxidation of methyl 3-<I>O</I>-benzyl-4,6-<I>O</I>-benzylidene-2-oximino-α-D-<I>arabino</I>-hexopyranoside (<B>5</B>) with trifluoroperoxyacetic acid afforded in 76% yield the corresponding 2-nitro-glucopyranoside (<B>6</B>) which has a twist-boat conformation in chloroform.
- 公益社団法人 日本化学会の論文
著者
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Sudoh Rokuro
Department of Chemistry, Faculty of Science, Tokyo Institute of Technology
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Sudoh Rokuro
Department of Chemistry, Tokyo Institute of Technology
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Takamoto Tetsuyoshi
Department of Chemistry, Tokyo Institute of Technology
関連論文
- Studies on Nitro Sugars. VI. Synthesis of Methyl 2-Deoxy-2-nitro-α-D-glucopyranoside Derivatives
- The preparation of isoxazole derivatives from a nitro sugar with dimethylsulfonium phenacylide.
- Formation of (4S,5R)-4-(nitrovinyl)-2-phenyl-1,3-dioxan-5-yl formate from methyl 4,6-O-benzylidene-2-deoxy-2-nitro-.BETA.-D-glucopyranoside.
- Stereochemistry of nucleophilic addition reactions. VIII. Preparation of 1,5-anhydro-4,6-O-benzylidene-2,3-dideoxy-3-nitro-D-erythro-hex-2-enitol and its reactions with some nucleophiles.
- Water-soluble acylating agents: Preparation of 2-acylthio-1-alkylpyridinium salts and acylation of phenols, acids, and/or amines with these salts in an aqueous phase.
- Stereochemistry of nucleophilic addition reactions. 6. Synthesis of isoxazoline N-oxide derivatives from methyl 4,6-O-benzylidene-2,3-dideoxy-3-nitro-.ALPHA.-D-erythro-hex-2-enopyranoside with some S-ylides.
- Stereochemistry of nucleophilic addition reactions. 10. Preparation of 2-C-diacetylmethyl and 2-C-acetylmethyl derivatives with the Altro, Gluco, and Manno configuration from methyl 4,6-O-benzylidene-2,3-dideoxy-3-nitro-.ALPHA.-D-erythro-hex-2-enopyranosi
- Preparation of .ALPHA.-nitro olefins from .ALPHA.-halo ketoximes.
- Stereochemistry of nucleophilic addition reactions. 5. Formation of stabilized ylides from methyl 4,6-O-benzylidene-2,3-dideoxy-3-nitro-.BETA.-D-erythro-hex-2-enopyranoside with some S-ylides; an important role of the nitro group for stabilization of the