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Please use this identifier to cite or link to this item:
http://ir.ncue.edu.tw/ir/handle/987654321/15028
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| Title: | Polyhydroxylated Indolines and Oxindoles from C-Glycosides via Sequential Henry Reaction, Michael Addition, and Reductive Amination/Amidation |
| Authors: | Zou, Wei;Wu, An-Tai;Bhasin, Milan;Sandbhor, Mahendra;Wu, Shih-Hsiung |
| Contributors: | 化學系 |
| Date: | 2007-03
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| Issue Date: | 2013-01-07T01:47:47Z
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| Publisher: | American Chemical Society |
| Abstract: | 6-Nitro-2‘-carbonyl-C-glycofuranosides synthesized via Henry reaction from 1-C-allyl 5-aldo-C-glycoside underwent an intramolecular Michael addition to afford nitrocyclohexanol derivatives in good to excellent yield. Reduction of the nitro group followed by intramolecular amination with ketone and aldehyde and amidation with ester produced indoline and oxindole derivatives, respectively, in excellent yield. |
| Relation: | J. Org. Chem., 72(7): 2686-2689 |
| Appears in Collections: | [化學系] 期刊論文
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