Heterobimetallic Pd-Sn catalysis: Highly selective intermolecular hydroarylation of ?-methyl substituted aryl alkenes
| dc.contributor.author | Das D. | en_US |
| dc.contributor.author | Pratihar S. | en_US |
| dc.contributor.author | Roy S. | en_US |
| dc.date.accessioned | 2025-02-17T04:49:58Z | |
| dc.date.issued | 2013 | |
| dc.description.abstract | The heterobimetallic catalyst [Pd(COD)Cl-SnCl3] efficiently promotes the intermolecular hydroarylation of ?-methyl substituted arenes (otherwise known to be dimerized/polymerized in presence of Lewis Acids) with indoles and other O-, S-heteroarenes leading to Markovnikov adducts. The reaction takes place under air and moisture insensitive condition. � 2012 Elsevier Ltd. All rights reserved. | en_US |
| dc.identifier.citation | 5 | en_US |
| dc.identifier.uri | http://dx.doi.org/10.1016/j.tetlet.2012.11.038 | |
| dc.identifier.uri | https://idr.iitbbs.ac.in/handle/2008/384 | |
| dc.language.iso | en | en_US |
| dc.subject | ?-Methyl substituted arene | en_US |
| dc.subject | Heterobimetallic catalysis | en_US |
| dc.subject | Hydroarylation | en_US |
| dc.subject | Indole | en_US |
| dc.subject | Regioselective C-C bond formation | en_US |
| dc.title | Heterobimetallic Pd-Sn catalysis: Highly selective intermolecular hydroarylation of ?-methyl substituted aryl alkenes | en_US |
| dc.type | Article | en_US |