Multi-catalysis reactions: Direct organocatalytic sequential one-pot synthesis of highly functionalized cyclopenta[b]chromen-1-ones
Multi-catalysis reactions: Direct organocatalytic sequential one-pot synthesis of highly functionalized cyclopenta[b]chromen-1-ones
| dc.contributor.author | Ramachary, Dhevalapally B. | |
| dc.contributor.author | Reddy, Y. Vijayendar | |
| dc.contributor.author | Kishor, Mamillapalli | |
| dc.date.accessioned | 2022-03-27T09:41:21Z | |
| dc.date.available | 2022-03-27T09:41:21Z | |
| dc.date.issued | 2008-11-13 | |
| dc.description.abstract | We have developed a new technology called multi-catalysis for the sequential one-pot synthesis of highly functionalized heterocycles. A practical and novel multi-component aniline-, self- and Brønsted acid-catalyzed selective process for the sequential one-pot synthesis of highly substituted 2-(2-hydroxy-aryl)-cyclopentane-1,3-diones, 3,9-dihydro-2H-cyclopenta[b]chromen- 1-ones and 3,3-dimethyl-2,3,4,9-tetrahydro-xanthen-1-ones is reported. Direct combination of aniline- and self-catalyzed cascade olefination-hydrogenation (O-H) and Brønsted acid-catalyzed cascade oxy-Michael-dehydration (OM-DH) of 1,3-diones, salicylic aldehydes and organic-hydrides is developed in one-pot to furnish the highly functionalized 3,9-dihydro-2H-cyclopenta[b]chromen-1-ones and 3,3-dimethyl-2,3,4,9-tetrahydro-xanthen-1-ones with high yields. © 2008 The Royal Society of Chemistry. | |
| dc.identifier.citation | Organic and Biomolecular Chemistry. v.6(22) | |
| dc.identifier.issn | 14770520 | |
| dc.identifier.uri | 10.1039/b812551a | |
| dc.identifier.uri | http://xlink.rsc.org/?DOI=b812551a | |
| dc.identifier.uri | https://dspace.uohyd.ac.in/handle/1/13199 | |
| dc.title | Multi-catalysis reactions: Direct organocatalytic sequential one-pot synthesis of highly functionalized cyclopenta[b]chromen-1-ones | |
| dc.type | Journal. Article | |
| dspace.entity.type |
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