期刊
JOURNAL OF ORGANIC CHEMISTRY
卷 88, 期 7, 页码 4799-4808出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.2c02969
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A facile, base-and catalyst-free synthesis of Morita-Baylis-Hillman and Rauhut-Currier adducts of fi-aminonitroalkenes with different electrophiles is reported. The reactions with ethyl glyoxylate, trifluoropyruvate, ninhydrin, vinyl sulfone, and N-tosylazadiene result in good to excellent yields of products at room temperature. The adducts of ninhydrin and fi-aminonitroalkene spontaneously cyclize to fused indenopyrroles. Gram-scale reactions and synthetic transformations of the adducts are also reported.
A facile, base-and catalyst-free synthesis of Morita???Baylis???Hillman and Rauhut???Currier adducts of fi-aminonitroalkenes with different electrophiles such as ethyl glyoxylate, trifluoropyruvate, ninhydrin, vinyl sulfone, and N-tosylazadiene is reported. The products are formed in good to excellent yields at room temperature with a broad substrate scope. The adducts of ninhydrin and fi-aminonitroalkene spontaneously cyclize to fused indenopyrroles. Gram-scale reactions and synthetic transformations of the adducts are also reported here.
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