Chemoselective reduction and transesterification of α-keto propargylic esters mediated by NaBH < inf > 4 < /inf > and CeCl < inf > 3 < /inf > 7H < inf > 2 < /inf > O
Chemoselective reduction and transesterification of α-keto propargylic esters mediated by NaBH < inf > 4 < /inf > and CeCl < inf > 3 < /inf > 7H < inf > 2 < /inf > O
| dc.contributor.author | Saravanan, Thangavel | |
| dc.contributor.author | Chadha, Anju | |
| dc.date.accessioned | 2022-03-27T08:56:03Z | |
| dc.date.available | 2022-03-27T08:56:03Z | |
| dc.date.issued | 2011-01-01 | |
| dc.description.abstract | An efficient one-pot synthesis of α-hydroxy propargylic esters by chemoselective reduction followed by transesterification using NaBH4 in combination with CeCl37H2O is described. © 2011 Taylor & Francis Group, LLC. | |
| dc.identifier.citation | Synthetic Communications. v.41(16) | |
| dc.identifier.issn | 00397911 | |
| dc.identifier.uri | 10.1080/00397911.2010.502993 | |
| dc.identifier.uri | http://www.tandfonline.com/doi/abs/10.1080/00397911.2010.502993 | |
| dc.identifier.uri | https://dspace.uohyd.ac.in/handle/1/12112 | |
| dc.subject | NaBH /CeCl 7H O 4 3 2 | |
| dc.subject | reduction | |
| dc.subject | transesterification | |
| dc.title | Chemoselective reduction and transesterification of α-keto propargylic esters mediated by NaBH < inf > 4 < /inf > and CeCl < inf > 3 < /inf > 7H < inf > 2 < /inf > O | |
| dc.type | Journal. Article | |
| dspace.entity.type |
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