Journal
BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY
Volume 18, Issue -, Pages 217-224Publisher
BEILSTEIN-INSTITUT
DOI: 10.3762/bjoc.18.25
Keywords
enantioselective; malonamate; nitroso aldol reaction; N-selectivity; Takemoto catalyst
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Funding
- CSIR-New Delhi
- 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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