Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/110172
Title: Enantioselective trimethylsilylcyanation of benzaldehyde using pyrrolidine-based chiral salen ligands
Authors: Serra, M. Elisa Silva 
Murtinho, Dina M. B. 
Goth, Albertino João Brito 
Keywords: Salens; tartaric acid; pyrrolidine; enantioselective; trimethylsilylcyanation; benzaldehyde
Issue Date: 2009
Publisher: Arkat USA
Project: Chymiotechnon 
REEQ/481/QUI/2006 
metadata.degois.publication.title: Arkivoc
metadata.degois.publication.volume: 2010
metadata.degois.publication.issue: 5
Abstract: The in situ formed Ti(IV) complexes of several pyrrolidine-based chiral salen ligands derived from natural (L)-tartaric acid were evaluated as catalysts in the enantioselective trimethylsilylcyanation of benzaldehyde. The catalysts were found to be very active, producing the corresponding product, O-trimethylsilylmandelonitrile, in high yields (>94%) and enantioselectivities of up to 88%.
URI: https://hdl.handle.net/10316/110172
ISSN: 1551-7012
DOI: 10.3998/ark.5550190.0011.507
Rights: openAccess
Appears in Collections:FCTUC Química - Artigos em Revistas Internacionais

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