Site-selective modification of peptides using rhodium and palladium catalysis: complementary electrophilic and nucleophilic arylation.
The site-selective modification of peptides containing dehydroalanine, tyrosine and tryptophan residues has been achieved using rhodium catalysed conjugate additions or palladium catalysed aryl-amination and -etherification reactions.
Hlavní autoři: | Chapman, C, Matsuno, A, Frost, C, Willis, M |
---|---|
Médium: | Journal article |
Jazyk: | English |
Vydáno: |
2007
|
Podobné jednotky
-
Aziridine electrophiles in the functionalisation of peptide chains with amine nucleophiles.
Autor: Spork, A, a další
Vydáno: (2015) -
Activation of Electrophile/Nucleophile Pair by a Nucleophilic and Electrophilic Solvation in a SNAr Reaction
Autor: Bruno Sánchez, a další
Vydáno: (2018-10-01) -
Graphene Oxide as an Electrophile for Carbon Nucleophiles
Autor: Swager, Timothy Manning, a další
Vydáno: (2012) -
Asymmetric electrophilic fluorocyclization with carbon nucleophiles.
Autor: Wolstenhulme, JR, a další
Vydáno: (2013) -
Pyridine sulfinates as general nucleophilic coupling partners in palladium-catalyzed cross-coupling reactions with aryl halides
Autor: Markovic, T, a další
Vydáno: (2017)