Literature DB >> 32011896

Rhodium(III)-Catalyzed C-H Alkenylation: Access to Maleimide-Decorated Tryptophan and Tryptophan-Containing Peptides.

Jingjing Peng1,2, Chunpu Li1,2, Mirzadavlat Khamrakulov1,2, Jiang Wang1,2, Hong Liu1,2.   

Abstract

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.

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Year:  2020        PMID: 32011896     DOI: 10.1021/acs.orglett.0c00086

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  1 in total

1.  Site-selective aqueous C-H acylation of tyrosine-containing oligopeptides with aldehydes.

Authors:  Marcos San Segundo; Arkaitz Correa
Journal:  Chem Sci       Date:  2020-10-06       Impact factor: 9.825

  1 in total

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