Synthesis of b-substituted alanines via Michael addition of nucleophiles to dehydroalanine derivatives

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Campo DC	Valor	Idioma
dc.contributor.author	Ferreira, Paula M. T.	-
dc.contributor.author	Maia, Hernâni L. S.	-
dc.contributor.author	Monteiro, Luís S.	-
dc.contributor.author	Sacramento, Joana	-
dc.contributor.author	Sebastião, Joana	-
dc.date.accessioned	2005-06-14T12:27:03Z	-
dc.date.available	2005-06-14T12:27:03Z	-
dc.date.issued	2000	-
dc.identifier.citation	“Journal of the chemical society. Perkin transactions”. 1 (2000) 3317-3324.	eng
dc.identifier.issn	1470-4358	por
dc.identifier.uri	https://hdl.handle.net/1822/2187	-
dc.description.abstract	Several b-substituted alanines are synthesised in high yields by a Michael addition of nucleophiles to N-acyl,N-tert-butyloxycarbonyl-dehydroalanine methyl ester, using mild reaction conditions and simple work-up procedures. The same method can be applied to dipeptides containing dehydroalanine.	eng
dc.language.iso	eng	eng
dc.publisher	Royal Society of Chemistry	eng
dc.rights	openAccess	eng
dc.title	Synthesis of b-substituted alanines via Michael addition of nucleophiles to dehydroalanine derivatives	eng
dc.type	article	eng
dc.peerreviewed	yes	eng
oaire.citationStartPage	3317	por
oaire.citationEndPage	3324	por
oaire.citationIssue	19	por
dc.identifier.doi	10.1039/b003353g	por
dc.subject.wos	Science & Technology	por
sdum.journal	Journal of the Chemical Society, Perkin Transactions 1	por
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