Please use this identifier to cite or link to this item: http://hdl.handle.net/1822/22066

TitleSynthesis of fluorescent alanines by a rhodium catalysed conjugate addition of arylboronic acids to dehydroalanine derivatives
Author(s)Ferreira, Paula M. T.
Monteiro, Luís S.
Castanheira, Elisabete M. S.
Pereira, Goreti
Frost, Christopher G.
KeywordsDehydroalanines
Rhodium-catalysis
Arylboronic acids
Conjugate addition
Fluorescent marker
Amino acids
Rhodium
Homogeneous catalysis
Fluorescent probes
Issue date2013
PublisherWiley-VCH Verlag
JournalEuropean Journal of Organic Chemistry
Abstract(s)Several arylalanine derivatives containing fluorescent groups were prepared in good yields using a rhodium catalysed conjugate addition of arylboronic acids to N,N-diprotected and N-monoprotected dehydroalanines. The best conditions for these reactions require the use of an excess of aryl boronic acid (4 equiv.), [Rh(COD)2]BF4 as catalyst and CsF as base in dioxane:H2O (10:1) at 110 ºC. These conditions were also applied to several dipeptides with dehydroalanine residues. The photophysical properties of some of the arylalanines were studied in three solvents of different polarity. Due to the absence of the, double bond, the absorption and fluorescence emission of the new compounds are dominated by the photophysical properties of the polycyclic aromatic fluorophores (naphthalene, phenanthrene and pyrene). Considering the relatively high fluorescence quantum yield of these compounds, some of them may be useful as fluorescent markers for peptides and proteins.
TypeArticle
URIhttp://hdl.handle.net/1822/22066
DOI10.1002/ejoc.201201198
ISSN1434-193X
Publisher versionhttp://dx.doi.org/10.1002/ejoc.201201198
Peer-Reviewedyes
AccessOpen access
Appears in Collections:CDF - FAMO - Artigos/Papers (with refereeing)
CDQuim - Artigos (Papers)

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