Direct oxidative installation of nitrooxy group at benzylic positions and its transformation into various functionalities |
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Authors: | Shin KamijoYuuki Amaoka Masayuki Inoue |
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Affiliation: | Graduate School of Pharmaceutical Sciences, The University of Tokyo, Hongo, Bunkyo-ku, Tokyo 113-0033, Japan |
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Abstract: | C-H Nitrooxylation at benzylic positions has been achieved by employing the N-hydroxyphthalimide (NHPI) catalyst/cerium(IV) ammonium nitrate (CAN) reagent system. The nitrooxy groups were demonstrated to function as tentative hydroxy protecting groups, as well as excellent leaving groups for N- and C-substitution reactions. Hence, the present method offers a unique way to synthesize diverse O-, N-, or C-functionalized benzylic compounds from simple alkyl aromatics. |
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Keywords: | Catalysis Nitrooxylation Benzylic position N-Hydroxyphthalimide Cerium(IV) ammonium nitrate |
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