A facile synthesis of 2H-indazoles under neat conditions and further transformation into aza-γ-carboline alkaloid analogues in a tandem one-pot fashion
We have described a facile, microwave-assisted, catalyst-free and solvent-free approach to 2H-indazoles and further developed a robust tandem one-pot metal-free strategy for C-C bond formation at the C-3 position of 2H-indazoles leading to a unique class of aza- gamma -carboline alkaloid analogues....
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| Veröffentlicht in: | RSC advances 2014-01, Vol.4 (65), p.34232-34236 |
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| container_end_page | 34236 |
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| container_issue | 65 |
| container_start_page | 34232 |
| container_title | RSC advances |
| container_volume | 4 |
| creator | Vidyacharan, Shinde Sagar, A. Chaitra, N. C. Sharada, Duddu S. |
| description | We have described a facile, microwave-assisted, catalyst-free and solvent-free approach to 2H-indazoles and further developed a robust tandem one-pot metal-free strategy for C-C bond formation at the C-3 position of 2H-indazoles leading to a unique class of aza- gamma -carboline alkaloid analogues. This straightforward expedient synthesis constitutes an interesting alternative to the existing conventional transition metal catalyzed reactions. |
| doi_str_mv | 10.1039/C4RA06838F |
| format | Article |
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This straightforward expedient synthesis constitutes an interesting alternative to the existing conventional transition metal catalyzed reactions.</description><subject>Alkaloids</subject><subject>Bonding</subject><subject>Carbon-carbon composites</subject><subject>Catalysts</subject><subject>Strategy</subject><subject>Synthesis</subject><subject>Transformations</subject><subject>Transition metals</subject><issn>2046-2069</issn><issn>2046-2069</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNpNkc1KAzEUhYMoWGo3PkGWIowmmZnMzLIUa4WCILoe7uTHRmeSmmQW7ZP4Hr6Hz2RKBb2bc-Ge83HhIHRJyQ0leXO7KJ7mhNd5vTxBE0YKnjHCm9N_-zmahfBG0vCSMk4n6HOONQjTKxx2Nm5UMAE7jdkqM1bC3vUq4NFK5bFVELFwVpponA0YrMR69CnjcfRgg3Z-gMMNGxsdhj1k31-ZAN-53liFoX-H3hmZkklfx0Q2FgOOiaQG7KzKti6md8ImQS7QmYY-qNmvTtHL8u55scrWj_cPi_k6E4wXMdOF0B1vKlYRSaiuOCkKLXnNBBV1BQxUo3ImOibKGiTnSnad0lVTQsUKBmU-RVdH7ta7j_RTbAcThOp7sMqNoaVVTkhdUX6wXh-twrsQvNLt1psB_K6lpD000P41kP8AG1N8Qg</recordid><startdate>20140101</startdate><enddate>20140101</enddate><creator>Vidyacharan, Shinde</creator><creator>Sagar, A.</creator><creator>Chaitra, N. 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| fulltext | fulltext |
| identifier | ISSN: 2046-2069 |
| ispartof | RSC advances, 2014-01, Vol.4 (65), p.34232-34236 |
| issn | 2046-2069 2046-2069 |
| language | eng |
| recordid | cdi_proquest_miscellaneous_1730087165 |
| source | Royal Society Of Chemistry Journals 2008- |
| subjects | Alkaloids Bonding Carbon-carbon composites Catalysts Strategy Synthesis Transformations Transition metals |
| title | A facile synthesis of 2H-indazoles under neat conditions and further transformation into aza-γ-carboline alkaloid analogues in a tandem one-pot fashion |
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