Taming furfurylcations for the synthesis of privileged structures and novel scaffolds†‡
| dc.contributor.author | Dhiman, Seema | |
| dc.contributor.author | Ramasastry, S.S.V. | |
| dc.date.accessioned | 2020-12-09T05:34:40Z | |
| dc.date.available | 2020-12-09T05:34:40Z | |
| dc.date.issued | 2013 | |
| dc.description.abstract | Furfuryl cations are generated via a highly efficient bismuth-catalyzed reaction of furfuryl alcohols. This systematic study provides insight on the reactivity profile of furfuryl cations towards nucleophilic substitution reactions. Novel C-C, C-N, C-O and C-S bond forming reactions of furfuryl cations have been developed, thus providing access to a diverse array of building blocks for further manipulations. | en_US |
| dc.identifier.citation | Organic and Biomolecular Chemistry, 11(26), pp. 4299-4303. | en_US |
| dc.identifier.other | https://doi.org/10.1039/C3OB40814K | |
| dc.identifier.uri | https://pubs.rsc.org/en/content/articlelanding/2013/ob/c3ob40814k#!divAbstract | |
| dc.identifier.uri | http://hdl.handle.net/123456789/2860 | |
| dc.language.iso | en | en_US |
| dc.publisher | Royal Society of Chemistry | en_US |
| dc.subject | Furfuryl cations | en_US |
| dc.subject | Alcohols | en_US |
| dc.subject | Highly efficient bismuth-catalyzed | en_US |
| dc.title | Taming furfurylcations for the synthesis of privileged structures and novel scaffolds†‡ | en_US |
| dc.type | Article | en_US |