Stereo- and Regio-Control of 1, 3-Dipolar Cycloaddition Reactions by the Aid of Lewis Acid Catalysts—Nitrone and aci-Nitro Compound Cycloadditions—
Author:
Affiliation:
1. Institute of Advanced Material Study, Kyushu University; 6-1 Kasugakoen, Kasuga-shi 816-8580 Japan
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/nikkashi/2000/3/2000_3_155/_pdf
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1. Functionalized nitrones. A highly stereoselective and regioselective synthesis of dl-retronecine
2. A New Route to Hexahydropyrrolizines Derivatives via Nonstabilized Ylide Generated from N-Methylpyrrolidine N-Oxide
3. Cycloaddition reactions of carbohydrate derivatives. Part IV. Synthesis of a tetrahydroxyindolizidine through a cyclic nitrone prepared from D-xylose.
4. Hydroxylated pyrrolizidines and indolizidines; synthesis using cycloaddition reactions of functionalized cyclic nitrones
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1. Electronic effects in 1,3-dipolar cycloaddition reactions of N-alkyl and N-benzyl nitrones with dipolarophiles;Org. Biomol. Chem.;2012
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4. Enantioselective 1,3-Dipolar Cycloaddition Reaction of Nitrones with α,β-Unsaturated Aldehydes Catalyzed by Cationic 3-Oxobutylideneaminatocobalt(III) Complexes;Bulletin of the Chemical Society of Japan;2003-11
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