2014-06-02T08:10:38Z
2021-11-01T06:10:14Z
2011-11-22
2014-05-30T11:35:20Z
The synthesis of various polycyclic systems containing a C3a-Ni 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.
Artículo
Versión presentada
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Productes naturals marins; Química heterocíclica; Aminoàcids; Síntesi de pèptids; Marine natural products; Heterocyclic chemistry; Amino acids; Peptide synthesis
Wiley-VCH
Versió preprint del document publicat a: http://dx.doi.org/10.1002/ejoc.201101057
European Journal of Organic Chemistry, 2012, vol. 2012, num. 1, p. 67-73
http://dx.doi.org/10.1002/ejoc.201101057
(c) Wiley-VCH Verlag GmbH & Co. KGaA, 2012