Baylis-Hillman acetates in organic synthesis: Convenient one-pot synthesis of α-carboline framework - A concise synthesis of neocryptolepine
Baylis-Hillman acetates in organic synthesis: Convenient one-pot synthesis of α-carboline framework - A concise synthesis of neocryptolepine
| dc.contributor.author | Basavaiah, Deevi | |
| dc.contributor.author | Mallikarjuna Reddy, Daggula | |
| dc.date.accessioned | 2022-03-27T09:01:19Z | |
| dc.date.available | 2022-03-27T09:01:19Z | |
| dc.date.issued | 2012-11-28 | |
| dc.description.abstract | A convenient, facile, and one-pot methodology for the synthesis of α-carbolines from Baylis-Hillman (BH) acetates, involving three steps (reactions), (1) mono alkylation of 2-nitroarylacetonitriles with BH-acetates, (2) reduction of nitro group into amino group using Fe/AcOH and (3) formation of two (five and six membered) rings, is presented. This methodology is successfully applied to the synthesis of bioactive alkaloid neocryptolepine. © 2012 The Royal Society of Chemistry. | |
| dc.identifier.citation | Organic and Biomolecular Chemistry. v.10(44) | |
| dc.identifier.issn | 14770520 | |
| dc.identifier.uri | 10.1039/c2ob26339d | |
| dc.identifier.uri | http://xlink.rsc.org/?DOI=c2ob26339d | |
| dc.identifier.uri | https://dspace.uohyd.ac.in/handle/1/12280 | |
| dc.title | Baylis-Hillman acetates in organic synthesis: Convenient one-pot synthesis of α-carboline framework - A concise synthesis of neocryptolepine | |
| dc.type | Journal. Article | |
| dspace.entity.type |
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