4.5 Article

Organocatalytic asymmetric nitroso aldol reaction of α-substituted malonamates

期刊

BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY
卷 18, 期 -, 页码 217-224

出版社

BEILSTEIN-INSTITUT
DOI: 10.3762/bjoc.18.25

关键词

enantioselective; malonamate; nitroso aldol reaction; N-selectivity; Takemoto catalyst

资金

  1. CSIR-New Delhi
  2. UGC-New Delhi

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The practical enantioselective N-selective nitroso aldol reaction of alpha-methylmalonamates with a nitrosoarene is reported. The Takemoto thiourea catalyst was employed to induce enantioselectivity, leading to the formation of optically active oxyaminated malonamates in reasonably good yields.
A practical enantioselective N-selective nitroso aldol reaction of alpha-methylmalonamates with a nitrosoarene is reported. The reaction employs the Takemoto thiourea catalyst for the induction of enantioselectivity, and the corresponding optically active oxyaminated malonamates were obtained in reasonably good yields.

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