Simple and efficient methods of synthesis of 3,3-diarylcyclobutanone and 3,3-diarylcyclobutylamine derivatives using the TiCl < inf > 4 < /inf > /R < inf > 3 < /inf > N reagent system
Simple and efficient methods of synthesis of 3,3-diarylcyclobutanone and 3,3-diarylcyclobutylamine derivatives using the TiCl < inf > 4 < /inf > /R < inf > 3 < /inf > N reagent system
| dc.contributor.author | Periasamy, Mariappan | |
| dc.contributor.author | Natarajan Jayakumar, K. | |
| dc.contributor.author | Bharathi, Pandi | |
| dc.date.accessioned | 2022-03-27T09:08:45Z | |
| dc.date.available | 2022-03-27T09:08:45Z | |
| dc.date.issued | 2005-07-08 | |
| dc.description.abstract | The iminium ions generated in situ by the oxidation of N,N-diisopropyl-N- benzylamine using iodine react with diaryl ketones in the presence of TiCl 4/R3N to give the corresponding 3,3-diarylcyclobutanones in moderate to good yields (49-86%). The 3,3-diarylcyclobutanone iminium ions formed in this transformation was reduced in situ with B2H 6 to produce the corresponding 3,3-diarylcyclobutylamines (52-79% yields), a class of compounds with potential antidepressant activity. In addition, a series of N,N-dimethyl-3,3-diarylcyclobutylamines were synthesized by the reductive amination of the corresponding 3,3-diarylcyclobutanone derivatives. © 2005 American Chemical Society. | |
| dc.identifier.citation | Journal of Organic Chemistry. v.70(14) | |
| dc.identifier.issn | 00223263 | |
| dc.identifier.uri | 10.1021/jo0504215 | |
| dc.identifier.uri | https://pubs.acs.org/doi/10.1021/jo0504215 | |
| dc.identifier.uri | https://dspace.uohyd.ac.in/handle/1/12488 | |
| dc.title | Simple and efficient methods of synthesis of 3,3-diarylcyclobutanone and 3,3-diarylcyclobutylamine derivatives using the TiCl < inf > 4 < /inf > /R < inf > 3 < /inf > N reagent system | |
| dc.type | Journal. Article | |
| dspace.entity.type |
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