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Domino Bischler-Napieralski - Michael reaction and oxidation, a new route to Coumarin-Pyrrole-Isoquinoline fused pentacycles
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| dc.contributor.author | Mandrekar, K.S. | |
| dc.contributor.author | Kadam, H.K. | |
| dc.contributor.author | Tilve, S.G. | |
| dc.date.accessioned | 2018-12-17T09:49:05Z | |
| dc.date.available | 2018-12-17T09:49:05Z | |
| dc.date.issued | 2018 | |
| dc.identifier.citation | European Journal of Organic Chemistry. 47; 2018; 6665-6670. | en_US |
| dc.identifier.uri | https://doi.org/10.1002/ejoc.201801244 | |
| dc.identifier.uri | http://irgu.unigoa.ac.in/drs/handle/unigoa/5548 | |
| dc.description.abstract | Lamellarin scaffold is synthesized by a metal free convergent route involving domino Bischler-Napieralski reaction - Michael reaction - oxidation sequence. Six lamellarin analogues were synthesised having substituent on aryl as well as coumarin ring A. | en_US |
| dc.publisher | Wiley-VCH | en_US |
| dc.subject | Chemistry | en_US |
| dc.title | Domino Bischler-Napieralski - Michael reaction and oxidation, a new route to Coumarin-Pyrrole-Isoquinoline fused pentacycles | en_US |
| dc.type | Journal article | en_US |
| dc.identifier.impf | y |
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School of Chemical Sciences [1049]