Iodine catalysed intramolecular C(sp3)-H functionalization: synthesis of 2,5-disubstituted oxazoles from N-arylethylamidesElectronic supplementary information (ESI) available: Detailed experimental procedures and spectroscopic data. See DOI: 10.1039/c5ra13441b
Iodine catalyzed synthesis of 2,5-disubstituted oxazoles from N -arylethylamides through intramolecular C(sp 3 )-H functionalization under metal-free conditions is described. The method is tolerable to a wide range of substrates having a variety of functional groups with moderate to good yields of t...
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Main Authors | , , , |
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Format | Journal Article |
Language | English |
Published |
05.08.2015
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Online Access | Get full text |
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Summary: | Iodine catalyzed synthesis of 2,5-disubstituted oxazoles from
N
-arylethylamides through intramolecular C(sp
3
)-H functionalization under metal-free conditions is described. The method is tolerable to a wide range of substrates having a variety of functional groups with moderate to good yields of the products.
Iodine catalyzed synthesis of 2,5-substituted oxazoles from
N
-arylethylamides through intramolecular C(sp
3
)-H functionalization under metal-free conditions is described. |
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Bibliography: | 10.1039/c5ra13441b Electronic supplementary information (ESI) available: Detailed experimental procedures and spectroscopic data. See DOI |
ISSN: | 2046-2069 |
DOI: | 10.1039/c5ra13441b |