Orthogonal protecting groups in the synthesis of tryptophanyl-hexahydropyrroloindoles
Data(s) |
03/06/2014
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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 | |
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 |