A novel arylation of arylacetic acid esters using tertiary arylamines and TiCl < inf > 4 < /inf >

dc.contributor.author Periasamy, Mariappan
dc.contributor.author KishoreBabu, N.
dc.contributor.author Jayakumar, Keela Natarajan
dc.date.accessioned 2022-03-27T09:09:14Z
dc.date.available 2022-03-27T09:09:14Z
dc.date.issued 2003-12-08
dc.description.abstract The reactions of arylacetic acid esters with tertiary arylamines in the presence of TiCl4 give α-arylated products in 65-90% yields, as well as 10-20% yields of the corresponding benzidines. © 2003 Elsevier Ltd. All rights reserved.
dc.identifier.citation Tetrahedron Letters. v.44(50)
dc.identifier.issn 00404039
dc.identifier.uri 10.1016/j.tetlet.2003.10.009
dc.identifier.uri https://www.sciencedirect.com/science/article/abs/pii/S0040403903024031
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12501
dc.subject Aryltitanium
dc.subject Cross coupling reactions
dc.subject Diaryl acetic esters
dc.subject Titanium enolates
dc.title A novel arylation of arylacetic acid esters using tertiary arylamines and TiCl < inf > 4 < /inf >
dc.type Journal. Article
dspace.entity.type
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