Photoredox catalyzed cascade CF addition/chemodivergent annulations of -alkenyl aryl ureas
Herein, we report a substrate-controlled cascade cyclization of o -alkenyl aryl ureas, an ambident nucleophile for constructing functionalized heterocycles such as 2-amino-1,3-benzoxazines and dihydroquinazolinones in a chemodivergent fashion using photoredox catalysis under mild conditions. The ver...
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Published in | Chemical communications (Cambridge, England) Vol. 58; no. 12; pp. 199 - 1993 |
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Main Authors | , , |
Format | Journal Article |
Published |
08.02.2022
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Online Access | Get full text |
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Summary: | Herein, we report a substrate-controlled cascade cyclization of
o
-alkenyl aryl ureas, an ambident nucleophile for constructing functionalized heterocycles such as 2-amino-1,3-benzoxazines and dihydroquinazolinones in a chemodivergent fashion using photoredox catalysis under mild conditions. The versatility of the method has been successfully demonstrated by applying this strategy to a wide range of substrates and for the synthesis of functionalized etifoxine drug derivatives.
Photoredox catalyzed cascade addition-chemodivergent annulations of
ortho
-alkenyl aryl ureas. |
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Bibliography: | 10.1039/d1cc06289a Electronic supplementary information (ESI) available. See DOI |
ISSN: | 1359-7345 1364-548X |
DOI: | 10.1039/d1cc06289a |