Synthesis of cis-2-aryl-3-pyrrolidine carboxylic esters via diastereoselective cyclization of γ-imino esters using a TiCl < inf > 4 < /inf > /Et < inf > 3 < /inf > N reagent system

dc.contributor.author Suresh, Surisetti
dc.contributor.author Periasamy, Mariappan
dc.date.accessioned 2022-03-27T09:08:59Z
dc.date.available 2022-03-27T09:08:59Z
dc.date.issued 2004-08-09
dc.description.abstract Facile synthesis of cis-2-aryl-3-pyrrolidine carboxylates from readily accessible γ-imino esters by intramolecular cyclization mediated by a TiCl4/Et3N reagent system is described. © 2004 Elsevier Ltd.
dc.identifier.citation Tetrahedron Letters. v.45(33)
dc.identifier.issn 00404039
dc.identifier.uri 10.1016/j.tetlet.2004.06.080
dc.identifier.uri https://www.sciencedirect.com/science/article/abs/pii/S0040403904013905
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12494
dc.subject Imino esters
dc.subject Intramolecular cyclization
dc.subject Pyrrolidines
dc.title Synthesis of cis-2-aryl-3-pyrrolidine carboxylic esters via diastereoselective cyclization of γ-imino esters using a TiCl < inf > 4 < /inf > /Et < inf > 3 < /inf > N reagent system
dc.type Journal. Article
dspace.entity.type
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