期刊
ORGANIC LETTERS
卷 14, 期 7, 页码 1834-1837出版社
AMER CHEMICAL SOC
DOI: 10.1021/ol300441z
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资金
- Skaggs Institute for Chemical Biology
A novel organocatalytic strategy for the synthesis of highly substituted spirocyclopentaneoxindoles was developed employing simple nitrostyrenes and 3-substituted oxindoles as starting materials. Michael-Henry cascade reactions, enabled through cinchona alkaloid organocatalysis, provided products in high yield and excellent enantioselectivity in a single step.
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