Orthogonal protecting groups in the synthesis of tryptophanyl-hexahydropyrroloindoles


Autoria(s): Ruiz Sanchis, Pau; Savina, Svetlana A.; Acosta, G.A.; Albericio Palomera, Fernando; Álvarez Domingo, Mercedes
Data(s)

03/06/2014

Resumo

The synthesis of various polycyclic systems containing a C3aNi bond between a hexahydropyrrolo[2,3-b]indole and an indole tryptophan is described here. A series of experiments were performed to determine the best combination of five orthogonal protecting groups and the best reaction conditions for formation of said bond, which is a common feature among many recently discovered marine natural products.

Identificador

http://hdl.handle.net/2072/231581

Idioma(s)

eng

Publicador

Wiley-VCH

Direitos

(c) Wiley-VCH Verlag GmbH & Co. KGaA, 2012

info:eu-repo/semantics/embargoedAccess

Palavras-Chave #Productes naturals marins #Química heterocíclica #Aminoàcids #Síntesi de pèptids #Marine natural products #Heterocyclic chemistry #Amino acids #Peptide synthesis
Tipo

info:eu-repo/semantics/article

info:eu-repo/semantics/submittedVersion