
Please use this identifier to cite or link to this item:
http://hdl.handle.net/123456789/2541
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DC Field | Value | Language |
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dc.contributor.author | Reddy, V. | - |
dc.contributor.author | Jadhav, A.S. | - |
dc.contributor.author | Anand, R.V. | - |
dc.date.accessioned | 2020-12-03T05:01:36Z | - |
dc.date.available | 2020-12-03T05:01:36Z | - |
dc.date.issued | 2016 | - |
dc.identifier.citation | European Journal of Organic Chemistry, 2016(3), pp. 453-458 | en_US |
dc.identifier.other | https://doi.org/10.1002/ejoc.201501390 | - |
dc.identifier.uri | https://chemistry-europe.onlinelibrary.wiley.com/doi/full/10.1002/ejoc.201501390 | - |
dc.identifier.uri | http://hdl.handle.net/123456789/2541 | - |
dc.description.abstract | Metal‐controlled domino reaction: A metal catalyzed regioselective aminative domino cyclization of 2‐alkynylbenzonitriles leading to 1‐aminoisoquinolines and/or 1‐aminoisoindolines was developed under solvent‐free conditions. It was found that the regioselectivity of the reaction was greatly influenced by the choice of metal catalyst. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Wiley-VCH Verlag | en_US |
dc.subject | Amination | en_US |
dc.subject | Heterocycles | en_US |
dc.subject | Isoquinolines | en_US |
dc.subject | Isoindolines | en_US |
dc.subject | Domino reactions | en_US |
dc.title | Catalyst‐Controlled Regioselective Approach to 1‐Aminoisoquinolines and/or 1‐Aminoisoindolines through Aminative Domino Cyclization of 2‐Alkynylbenzonitriles | en_US |
dc.type | Article | en_US |
Appears in Collections: | Research Articles |
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