A Convenient Synthesis of C-3-Aryloxymethyl Imidazo[1,2-a]Pyridine Derivatives
Imidazo[1,2-a]pyridine-based tosylhydrazone was prepared and treated with K2CO3 in dioxane at 110°C to generate the corresponding carbene in situ. It was coupled with a variety of aryl alcohols in one pot to obtain a series of imidazo[1,2-a]pyridine derivatives possessing aryl ether moiety at C-3 po...
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| Format: | Article |
| Language: | English |
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Wiley
2013-01-01
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| Series: | Journal of Chemistry |
| Online Access: | http://dx.doi.org/10.1155/2013/296792 |
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| author | Sridevi Kona Rama Suresh Ravi Venkata N. R. Chava Ramu Sridhar Perali |
| author_facet | Sridevi Kona Rama Suresh Ravi Venkata N. R. Chava Ramu Sridhar Perali |
| author_sort | Sridevi Kona |
| collection | DOAJ |
| description | Imidazo[1,2-a]pyridine-based tosylhydrazone was prepared and treated with K2CO3 in dioxane at 110°C to generate the corresponding carbene in situ. It was coupled with a variety of aryl alcohols in one pot to obtain a series of imidazo[1,2-a]pyridine derivatives possessing aryl ether moiety at C-3 position. |
| format | Article |
| id | doaj-art-572f243e7c9b4645bef99a5cb2554c39 |
| institution | OA Journals |
| issn | 2090-9063 2090-9071 |
| language | English |
| publishDate | 2013-01-01 |
| publisher | Wiley |
| record_format | Article |
| series | Journal of Chemistry |
| spelling | doaj-art-572f243e7c9b4645bef99a5cb2554c392025-08-20T02:05:57ZengWileyJournal of Chemistry2090-90632090-90712013-01-01201310.1155/2013/296792296792A Convenient Synthesis of C-3-Aryloxymethyl Imidazo[1,2-a]Pyridine DerivativesSridevi Kona0Rama Suresh Ravi1Venkata N. R. Chava2Ramu Sridhar Perali3School of Chemistry, University of Hyderabad, Andhra Pradesh, Hyderabad 500046, IndiaSchool of Chemistry, University of Hyderabad, Andhra Pradesh, Hyderabad 500046, IndiaDepartment of Chemistry, AG & SG Siddhartha Arts and Science College, Andhra Pradesh, Vuyyuru 521165, IndiaSchool of Chemistry, University of Hyderabad, Andhra Pradesh, Hyderabad 500046, IndiaImidazo[1,2-a]pyridine-based tosylhydrazone was prepared and treated with K2CO3 in dioxane at 110°C to generate the corresponding carbene in situ. It was coupled with a variety of aryl alcohols in one pot to obtain a series of imidazo[1,2-a]pyridine derivatives possessing aryl ether moiety at C-3 position.http://dx.doi.org/10.1155/2013/296792 |
| spellingShingle | Sridevi Kona Rama Suresh Ravi Venkata N. R. Chava Ramu Sridhar Perali A Convenient Synthesis of C-3-Aryloxymethyl Imidazo[1,2-a]Pyridine Derivatives Journal of Chemistry |
| title | A Convenient Synthesis of C-3-Aryloxymethyl Imidazo[1,2-a]Pyridine Derivatives |
| title_full | A Convenient Synthesis of C-3-Aryloxymethyl Imidazo[1,2-a]Pyridine Derivatives |
| title_fullStr | A Convenient Synthesis of C-3-Aryloxymethyl Imidazo[1,2-a]Pyridine Derivatives |
| title_full_unstemmed | A Convenient Synthesis of C-3-Aryloxymethyl Imidazo[1,2-a]Pyridine Derivatives |
| title_short | A Convenient Synthesis of C-3-Aryloxymethyl Imidazo[1,2-a]Pyridine Derivatives |
| title_sort | convenient synthesis of c 3 aryloxymethyl imidazo 1 2 a pyridine derivatives |
| url | http://dx.doi.org/10.1155/2013/296792 |
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