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1.
J Am Chem Soc ; 130(31): 10084-5, 2008 Aug 06.
Artigo em Inglês | MEDLINE | ID: mdl-18613686

RESUMO

Enantioenriched 3-pyrrolines have been synthesized by highly enantioselective Fesulphos-Cu-catalyzed 1,3-dipolar cycloaddition of azomethine ylides with trans-1,2-bisphenylsulfonyl ethylene, followed by reductive sulfonyl elimination. High levels of reactivity, exoselectivity, and enantioselectivity have been accomplished for a variety of substituted azomethine ylides. This cycloaddition-desulfonylation strategy has been applied as a key step in the enantioselective synthesis of a biologically active C-azanucleoside.

2.
J Org Chem ; 72(14): 5129-38, 2007 Jul 06.
Artigo em Inglês | MEDLINE | ID: mdl-17555353

RESUMO

Tamandarins A and B are a class of marine natural cyclodepsipeptides with structures and biological activities closely related to those of the didemnins. The easier synthetic access to tamandarins accelerates the preparation of new macrocyclic derivatives of this family of antitumor, antiviral, and immunosuppressive compounds. The optimization of the previously reported synthetic route to tamandarins by changing the macrolactamization site from Nst1 and Thr6 to Pro4 and N,O-Me2Tyr5 residues led to a significant improvement in the reaction yield. Using this new synthetic approach, four new macrocyclic analogues of tamandarin B were prepared and evaluated for anticancer activity. These results provide further insight into the structure-activity relationship of the tamandarins and didemnins.


Assuntos
Depsipeptídeos/química , Depsipeptídeos/toxicidade , Aminoácidos/química , Linhagem Celular Tumoral , Sobrevivência Celular/efeitos dos fármacos , Depsipeptídeos/síntese química , Humanos , Metilação , Estrutura Molecular , Naftalenos/química
3.
Org Lett ; 8(3): 511-4, 2006 Feb 02.
Artigo em Inglês | MEDLINE | ID: mdl-16435872

RESUMO

[structure: see text]. The synthesis of two tamandarin B analogues in which the N,O-Me2Tyr5 unit was replaced by N-Me-phenylalanine (N-MePhe5) and (S)-2-(methylamino)-3-(naphthalen-2-yl)propanoic acid (N-MeNaphth5) is described. The choice of the macrocyclization site was crucial to achieve satisfactory macrolactamization. Coupling between norstatine (Nst1) and threonine (Thr6) afforded only a 15% yield, while lactamization between proline (Pro4) and the aromatic moiety could be achieved in 65% yield.


Assuntos
Antineoplásicos/síntese química , Antineoplásicos/farmacologia , Depsipeptídeos/síntese química , Depsipeptídeos/farmacologia , Antineoplásicos/química , Depsipeptídeos/química , Doxorrubicina/farmacologia , Resistencia a Medicamentos Antineoplásicos/efeitos dos fármacos , Ensaios de Seleção de Medicamentos Antitumorais , Humanos , Estrutura Molecular , Peptídeos Cíclicos , Células Tumorais Cultivadas
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