Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/127746
Title: Simultaneous cyclization and derivatization of peptides using cyclopentenediones
Author: Brun Cubero, Omar
Archibald, L. J.
Agramunt, Jordi
Pedroso Muller, Enrique
Grandas Sagarra, Anna
Keywords: Pèptids
Cisteïna
Estructura molecular
Peptides
Cysteine
Molecular structure
Issue Date: 3-Mar-2017
Publisher: American Chemical Society
Abstract: Unprotected linear peptides containing N-terminal cysteines and another cysteine residue can be simultaneously cyclized and derivatized using 2,2-disubstituted cyclopentenediones. High yields of cyclic peptide conjugates may be obtained in short reaction times using only a slight excess of the cyclopentenedione moiety under TEMPO catalysis and in the presence of LiCl.
Note: Versió postprint del document publicat a: https://doi.org/10.1021/acs.orglett.6b03825
It is part of: Organic Letters, 2017, vol. 19, num. 5, p. 992-995
URI: http://hdl.handle.net/2445/127746
Related resource: https://doi.org/10.1021/acs.orglett.6b03825
ISSN: 1523-7060
Appears in Collections:Articles publicats en revistes (Química Inorgànica i Orgànica)

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