First example of a heterobimetallic 'Pd-Sn' catalyst for direct activation of alcohol: Efficient allylation, benzylation and propargylation of arenes, heteroarenes, active methylenes and allyl-Si nucleophiles
| dc.contributor.author | Das D. | en_US |
| dc.contributor.author | Pratihar S. | en_US |
| dc.contributor.author | Roy U.K. | en_US |
| dc.contributor.author | Mal D. | en_US |
| dc.contributor.author | Roy S. | en_US |
| dc.date.accessioned | 2025-02-17T04:44:12Z | |
| dc.date.issued | 2012 | |
| dc.description.abstract | Arenes, heteroarenes, 1,3-dicarbonyls and organosilicon nucleophiles undergo highly efficient alkylation with allylic, propargylic and benzylic alcohols in the presence of a new 'Pd-Sn' bimetallic catalyst in nitromethane; water being the sole byproduct. The plausible mechanism of alkylation and the intermediacy of ether has been enumerated. � 2012 The Royal Society of Chemistry. | en_US |
| dc.identifier.citation | 28 | en_US |
| dc.identifier.uri | http://dx.doi.org/10.1039/c2ob25275a | |
| dc.identifier.uri | https://idr.iitbbs.ac.in/handle/2008/220 | |
| dc.language.iso | en | en_US |
| dc.title | First example of a heterobimetallic 'Pd-Sn' catalyst for direct activation of alcohol: Efficient allylation, benzylation and propargylation of arenes, heteroarenes, active methylenes and allyl-Si nucleophiles | en_US |
| dc.type | Article | en_US |