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Adição nucleofílica em alilaminas promovida por complexos de paládio (II)

o presente trabalho relata o estudo das reações de carbo- e alcoxipaladação de olefinas funcionalizadas. Para tal propósito, foram sintetizadas as alilaminas 4,N,N-dibenzilamino-5-metilexen-2-enoato de metila (138), 3,N,N-dibenzilaminoprop-l-eno (111) e 3,N,N-(R,R)-α,α-dimetildibenzilaminoprop-l-eno(114). A alilamina (138), desativada pelo grupo carbóxi, e a alilamina (114), devido a presença dos grupos volumosos dimetildibenzil ligados ao nitrogênio, não sofrem adição nucleofílica, na presença de sais de paládio (II). Entretanto, a alilamina (111), na presença de PdCl2(PhCN) 2 e carboxilatos, produz seletivamente complexos paladociclos de cinco membros. / We present the synthesis of chiral and achiral allylic amines derived from α-amino acids. The carbo- and alcoxy-palladation of these allylic amines have been investigated. The allylic amine methyl 4,N,N-dibenzylamino-5-methylhexen-2-enoate (138), desactivated by carboxy groups, and the allylic amine 3,N,N-(R,R)-α,αdimethyldibenzylaminoprop-l-ene (114), with the bulky group α,α-dimethyldibenzyl attached at amino group, did not undergo nucleophilic additions, in the presence of Pd(II) salts. However, the 3,N,N-dibenzylaminoprop-l-ene (111), in the presence of PdCl2(PhCN)2 and carboxilates, produces selectively five-membered palladocyclic complexes.

Identiferoai:union.ndltd.org:IBICT/oai:lume.ufrgs.br:10183/24990
Date January 1994
CreatorsSchenato, Rossana Angelica
ContributorsDupont, Jairton
Source SetsIBICT Brazilian ETDs
LanguagePortuguese
Detected LanguageUnknown
Typeinfo:eu-repo/semantics/publishedVersion, info:eu-repo/semantics/masterThesis
Formatapplication/pdf
Sourcereponame:Biblioteca Digital de Teses e Dissertações da UFRGS, instname:Universidade Federal do Rio Grande do Sul, instacron:UFRGS
Rightsinfo:eu-repo/semantics/openAccess

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