Selective N‐Arylation of p ‐Aminophenylalanine in Unprotected Peptides with Organometallic Palladium Reagents-Reference-Cited by-同舟云学术

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Selective N‐Arylation of p ‐Aminophenylalanine in Unprotected Peptides with Organometallic Palladium Reagents

Published:2021-06-26 Issue:31 Volume:133 Page:17065-17068
ISSN:0044-8249
Container-title:Angewandte Chemie
language:en
Short-container-title:Angew. Chem.

Author:

Mallek Aaron J.¹^ORCID,Pentelute Bradley L.¹,Buchwald Stephen L.¹^ORCID

Affiliation:

1. Department of Chemistry Massachusetts Institute of Technology 77 Massachusetts Avenue Cambridge MA 02139 USA

Funder

National Institutes of Health

Bristol-Myers Squibb

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ange.202104780

Reference33 articles.

1. Advances in Chemical Protein Modification

2. Towards the next generation of biomedicines by site-selective conjugation

3. Residue-Specific Peptide Modification: A Chemist’s Guide

4. Site-Selective Lysine Modification of Native Proteins and Peptides via Kinetically Controlled Labeling

5. Iminoboronates: A New Strategy for Reversible Protein Modification

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Selective Stepwise Arylation of Unprotected Peptides by Pt ^IV Complexes;Angewandte Chemie International Edition;2022-06-02

2. Selective Stepwise Arylation of Unprotected Peptides by Pt ^IV Complexes;Angewandte Chemie;2022-06-02

3. Pd(II)‐Mediated C−H Activation for Cysteine Bioconjugation;Chemistry – A European Journal;2022-01-12

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