
Please use this identifier to cite or link to this item:
http://hdl.handle.net/123456789/2068
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DC Field | Value | Language |
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dc.contributor.author | Yadav, S. | - |
dc.contributor.author | Hazra, R. | - |
dc.contributor.author | Singh, Animesh | - |
dc.contributor.author | Ramasastry, S.S.V. | - |
dc.date.accessioned | 2020-11-23T11:22:49Z | - |
dc.date.available | 2020-11-23T11:22:49Z | - |
dc.date.issued | 2019 | - |
dc.identifier.citation | Organic Letters, 21(9),pp.2983-2987. | en_US |
dc.identifier.other | https://doi.org/10.1021/acs.orglett.9b00410 | - |
dc.identifier.uri | https://pubs.acs.org/doi/10.1021/acs.orglett.9b00410 | - |
dc.identifier.uri | http://hdl.handle.net/123456789/2068 | - |
dc.description.abstract | An efficient palladium-catalyzed intramolecular Trost–Oppolzer type Alder-ene strategy was developed for the synthesis of carbazoles and cyclopenta[b]indoles from easily accessible(3-allyl-1H-indol-2-yl)methyl acetates. This strategy was extended for the synthesis of naphthalenes and dibenzobenzofurans as well. In addition, a short synthesis of antibacterial and antifungal natural product glycozoline and its analogues was also achieved. | en_US |
dc.language.iso | en | en_US |
dc.publisher | American Chemical Society | en_US |
dc.subject | Intramolecular | en_US |
dc.subject | Trost–Oppolzer | en_US |
dc.subject | Antifungal | en_US |
dc.subject | Natural | en_US |
dc.title | Substituent-Guided Palladium-Ene Reaction for the Synthesis of Carbazoles and Cyclopenta[b]indoles | en_US |
dc.type | Article | en_US |
Appears in Collections: | Research Articles |
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