Rhodium(III)-Catalyzed C-H Alkenylation: Access to Maleimide-Decorated Tryptophan and Tryptophan-Containing Peptides.
Journal
Organic letters
ISSN: 1523-7052
Titre abrégé: Org Lett
Pays: United States
ID NLM: 100890393
Informations de publication
Date de publication:
21 02 2020
21 02 2020
Historique:
pubmed:
6
2
2020
medline:
18
11
2020
entrez:
4
2
2020
Statut:
ppublish
Résumé
Maleimide is widely applied in many fields, especially in antibody-drug conjugations and peptide drugs. Herein, we develop a strategy for the C-H alkenylation of tryptophan and tryptophan-containing peptides, providing a synthetic route of decorating maleimide on peptides. The method has a high tolerance of functional groups and protecting groups. Furthermore, this method was applied to prepare peptide conjugation with molecules such as drugs and fluorescence probes. Moreover, macrocyclic peptides were obtained via this reaction.
Identifiants
pubmed: 32011896
doi: 10.1021/acs.orglett.0c00086
doi:
Substances chimiques
Alkenes
0
Maleimides
0
Peptides
0
maleimide
2519R1UGP8
Tryptophan
8DUH1N11BX
Rhodium
DMK383DSAC
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM