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Synthesis and tuberculostatic activity of adducts of aryl- and aryloxyfurans with acetylenedicarboxylic ester, maleic anhydride, and N-phenylmaleimide

✍ Scribed by A. F. Oleinik; E. V. Adamskaya; K. Yu. Novitskii; N. P. Solov'eva; N. I. Fadeeva; I. N. Degtyareva; N. B. Lapaeva; G. N. Pershin

Book ID: 112407450
Publisher: Springer
Year: 1980
Tongue: English
Weight: 309 KB
Volume: 14
Category: Article
ISSN: 0091-150X
DOI: 10.1007/bf00777382

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## Abstract Isocyanides, dialkyl acetylenedicarboxylates (=dialkyl but‐2‐ynedioates), and anhydrides such as maleic anhydride (=furan‐2,3‐dione) or citraconic anhydride (=3‐methylfuran‐2,3‐dione) react in one pot to afford novel iminospiro‐__γ__‐lactones in fairly good yields at room temperature (_