Phosphoramide-Catalyzed Michael Addition of Oxindoles to Nitroolefins
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17
摘要:
Zhou and co-workers present a highly efficient asymmetric Michael addition of oxindoles to nitroolefins using phosphoramide catalyst A . The authors developed the new catalyst A on the basis of the cinchona alkaloid structure. Excellent diastereoselectivities and enantioselectivities were observed under the reaction conditions.
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DOI:
10.1055/s-0031-1289265
年份:
2011
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