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Multisubstituted isoquinoline and pyridine N-oxides have been prepared by Rh(III)-catalyzed cyclization of oximes and diazo compounds via aryl and vinylic C-H activation. This intermolecular annulation involving tandem C-H activation, cyclization, and condensation steps proceeds under mild conditions, obviates the need for oxidants, releases N2 and H2O as the byproducts, and displays a broad substituent scope.
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Zhuangzhi Shi
Dennis C. Koester
Melissa Boultadakis‐Arapinis
Journal of the American Chemical Society
University of Münster
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Shi et al. (Fri,) studied this question.
synapsesocial.com/papers/6a10788310ed65f1d0fce1ae — DOI: https://doi.org/10.1021/ja406338r