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Isopropanol and potassium tert-butoxide promoted intramolecular direct sp2 C–H functionalization: an expedient synthesis of 1,2,3-triazole annulated chromens and quinolones
[Display omitted] A series of 1,2,3-triazole annulated chromen and quinolone derivatives have been synthesized by means of direct sp2 C–H functionalization in the presence of iso-propanol and potassium tert-butoxide. The reaction proceeds through homolytic aromatic substitution (HAS). This efficient...
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Published in: | Tetrahedron letters 2015-10, Vol.56 (44), p.6123-6127 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | [Display omitted]
A series of 1,2,3-triazole annulated chromen and quinolone derivatives have been synthesized by means of direct sp2 C–H functionalization in the presence of iso-propanol and potassium tert-butoxide. The reaction proceeds through homolytic aromatic substitution (HAS). This efficient as well as simple C–H functionalization methodology offers a straightforward route to 1,2,3-triazole annulated oxygen and nitrogen heterocycles. |
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ISSN: | 0040-4039 1873-3581 |
DOI: | 10.1016/j.tetlet.2015.09.096 |