A new approach to the synthesis of di- and tripeptides with unnatural amino acids using organozinc chemistry
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference28 articles.
1. C-Alkylation of Peptides through Polylithiated and LiCl-Solvated Derivatives Containing Sarcosine Li-Enolate Units
2. Peptide Enolates.C-Alkylation of Glycine Residues in linear tri-, tetra-, and pentapeptidesvia dilithium azadienediolates
3. Stereoselective alkylation of glycine units in dipeptide derivatives. "Chirality transfer" via a pivalaldehyde N,N-acetal center
4. Asymmetric alkylations of a phenylalanylglycinate equivalent. Novel route to dipeptides bearing .alpha.-alkyl-.alpha.-amino acid residues
5. Free-radical addition to di- and tripeptides containing dehydroalanine residues
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2. Umpolung Ala B Reagents for the Synthesis of Non‐Proteogenic Amino Acids, Peptides and Proteins**;Angewandte Chemie International Edition;2022-06-23
3. Umpolung Ala B Reagents for the Synthesis of Non‐Proteogenic Amino Acids, Peptides and Proteins**;Angewandte Chemie;2022-06-22
4. Blue light-promoted N–H insertion of amides, isatins, sulfonamides and imides into aryldiazoacetates: Synthesis of unnatural α-aryl amino acid derivatives;Tetrahedron;2020-12
5. C–C Bond Formation by Cross-Coupling;Reference Module in Chemistry, Molecular Sciences and Chemical Engineering;2013
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