Oxidative cycloaddition of hydroxamic acids with dienes or guaiacols mediated by iodine(III) reagents

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Abstract

[Bis(trifluoroacetoxy)iodo]benzene (BTI) and (diacetoxyiodo)benzene (DIB) efficiently promote the formation of acylnitroso species from hydroxamic acids in the presence of various dienes to give the corresponding hetero-Diels-Alder (HDA) adducts in moderate to high yields. The present method could be applied to the HDA reactions of acylnitroso species with o-benzoquinones generated by the oxidative dearomatization of guaiacols.

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Shimizu, H., Yoshimura, A., Noguchi, K., Nemykin, V. N., Zhdankin, V. V., & Saito, A. (2018). Oxidative cycloaddition of hydroxamic acids with dienes or guaiacols mediated by iodine(III) reagents. Beilstein Journal of Organic Chemistry, 14, 531–536. https://doi.org/10.3762/bjoc.14.39

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