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- W2333479000 abstract "Methyl 5-nitro-2-furylpropiolate was treated with alicyclic secondary amines to obtain the corresponding 5-nitro-2-furyl-β-aminoacrylates in a yield over 50%. Their structures were discussed based on their NMR, IR, and UV spectra. Though such amine-addition products were obtained with diethylamine, phenyl hydrazine, and ammonia, triethylamine, aniline, and N-methylaniline gave a different line of products.Intramolecular Diels-Alder reactions were attempted using 5-nitro-2-furylpropiolic acid in the presence of acetic anhydride or using its allyl ester. The former afforded only its anhydride, whereas the latter, the desired cyclic product." @default.
- W2333479000 created "2016-06-24" @default.
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- W2333479000 date "1968-01-01" @default.
- W2333479000 modified "2023-09-29" @default.
- W2333479000 title "Reactions of 5-Nitro-2-furylpropiolic Acid Derivatives. I" @default.
- W2333479000 doi "https://doi.org/10.5059/yukigoseikyokaishi.26.264" @default.
- W2333479000 hasPublicationYear "1968" @default.
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