Toward understanding the scope of Baylis-Hillman reaction: Synthesis of 3-(2- hydroxyphenyl)indolin-2-ones and polycyclic fused furans
Toward understanding the scope of Baylis-Hillman reaction: Synthesis of 3-(2- hydroxyphenyl)indolin-2-ones and polycyclic fused furans
| dc.contributor.author | Basavaiah, Deevi | |
| dc.contributor.author | Roy, Suparna | |
| dc.contributor.author | Das, Utpal | |
| dc.date.accessioned | 2022-03-27T09:01:30Z | |
| dc.date.available | 2022-03-27T09:01:30Z | |
| dc.date.issued | 2010-07-24 | |
| dc.description.abstract | A facile one-pot synthesis of 3-(2-hydroxyphenyl)indolin-2-ones has been developed via the TiCl4-me- diated Baylis-Hillman (B-H) reaction of N-substituted isatins and cyclohex-2-enone, followed by treatment of the in situ generated B-H alcohols with aq HBr. Baylis-Hillman reaction of aromatic cyclic 1, 2-diones with cycloalk-2-enones under the influence of TiCl4 has been successfully performed and the resulting Baylis-Hillman adducts have been conveniently transformed into pentacyclic and hexacyclic fused furan derivatives. © 2010 Elsevier Ltd. All rights reserved. | |
| dc.identifier.citation | Tetrahedron. v.66(30) | |
| dc.identifier.issn | 00404020 | |
| dc.identifier.uri | 10.1016/j.tet.2010.05.087 | |
| dc.identifier.uri | https://www.sciencedirect.com/science/article/abs/pii/S0040402010008410 | |
| dc.identifier.uri | https://dspace.uohyd.ac.in/handle/1/12286 | |
| dc.subject | 2-diones | |
| dc.subject | 3-(2-Hydroxyphenyl)indolin-2-ones | |
| dc.subject | Baylis-Hillman reaction | |
| dc.subject | Cyclic 1 | |
| dc.subject | Cycloalk-2-enones | |
| dc.subject | Polycyclic fused furans | |
| dc.title | Toward understanding the scope of Baylis-Hillman reaction: Synthesis of 3-(2- hydroxyphenyl)indolin-2-ones and polycyclic fused furans | |
| dc.type | Journal. Article | |
| dspace.entity.type |
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