Abstract
Reactions of (N-isocyanimino)triphenylphosphorane with (1R)-(-)- campherchinon in the presence of aromatic carboxylic acids proceed smoothly at room temperature and in neutral conditions to afford sterically congested 1,3,4-oxadiazole derivatives in high yields. The reaction proceeds smoothly and cleanly under mild conditions and no side reactions were observed.
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Ramazani, A., Nasrabadi, F. Z., Abdian, B., & Rouhani, M. (2012). One-pot, three-component synthesis of fully substituted 1,3,4-oxadiazole derivatives from (N-isocyanoimino)triphenylphosphorane, aromatic carboxylic acids and (1R)-(-)-campherchinon. Bulletin of the Korean Chemical Society, 33(2), 453–458. https://doi.org/10.5012/bkcs.2012.33.2.453
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