Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/104902
Type: Artigo de periódico
Title: Synthesis Of Conformationally Restricted Acetylcholine Analogues. Comparing Lipase-mediated Resolution With Simulated Moving Bed Chromatography Of Arylated β-hydroxy-pyrrolidines
Author: Barreto R.d.L.
Carpes M.J.S.
Santana C.C.
Correia C.R.D.
Abstract: The enantiodivergent synthesis of new, conformationally restricted acetylcholine analogues was accomplished using arylated endocyclic enecarbamates as key intermediates. Stereoselective hydroboration of the aryl enecarbamates provided the corresponding aryl-β-hydroxy-pyrrolidines. Acetylation, deprotection, followed by N-bismethylation, led to the desired betaine products. The kinetic resolution of the intermediate alcohols was performed by lipase-mediated hydrolysis of its acetate derivatives, resulting in excellent enantioselectivities (E > 100). An enzymatic enantiopreference predicted by the Kazlauskas's model was confirmed following Riguera's protocol. Finally, chromatographic resolution of racemic alcohol 5a was evaluated by semi-preparative scale chiral simulated moving bed chromatography and its performance compared with biocatalysis. © 2007 Elsevier Ltd. All rights reserved.
Editor: 
Rights: fechado
Identifier DOI: 10.1016/j.tetasy.2007.01.030
Address: http://www.scopus.com/inward/record.url?eid=2-s2.0-33847632583&partnerID=40&md5=d19b63ea9fe830d27f85269fc1c37d7e
Date Issue: 2007
Appears in Collections:Unicamp - Artigos e Outros Documentos

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