Aziridine-2-carboxylic acid-containing peptides: application to solution- and solid-phase convergent site-selective peptide modification.
about
Sublancin is not a lantibiotic but an S-linked glycopeptideImproved production of sublancin via introduction of three characteristic promoters into operon clusters responsible for this novel distinct glycopeptide biosynthesisSite-selective modification of peptides: From "customizable units" to novel α-aryl and α-alkyl glycine derivatives, and components of branched peptides.Solid-phase synthesis, cyclization, and site-specific functionalization of aziridine-containing tetrapeptides.Rings, radicals, and regeneration: the early years of a bioorganic laboratorySynthetic strategies for polypeptides and proteins by chemical ligation.Recent progress in the field of neoglycoconjugate chemistry.Modern tools for the chemical ligation and synthesis of modified peptides and proteins.Chemoselective Reactions for the Synthesis of Glycoconjugates from Unprotected Carbohydrates.Three-component synthesis of highly functionalized aziridines containing a peptide side chain and their one-step transformation into β-functionalized α-ketoamides.Sigmatropic rearrangements as tools for amino acid and peptide modification: application of the allylic sulfur ylide rearrangement to the preparation of neoglycoconjugates and other conjugates.Synthesis of peptide macrocycles using unprotected amino aldehydes.Dechalcogenative allylic selenosulfide and disulfide rearrangements: complementary methods for the formation of allylic sulfides in the absence of electrophiles. Scope, limitations, and application to the functionalization of unprotected peptides inChemical synthesis of the S-linked glycopeptide, sublancin.Metal-Free, Site-Selective Peptide Modification by Conversion of "Customizable" Units into β-Substituted Dehydroamino Acids.Protecting group free synthesis of glycosyl thiols from reducing sugars in water; application to the production of N-glycan glycoconjugates.Aziridine-Mediated Ligation at Phenylalanine and Tryptophan Sites.The effect of backbone flexibility on site-selective modification of macrocycles.
P2860
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P2860
Aziridine-2-carboxylic acid-containing peptides: application to solution- and solid-phase convergent site-selective peptide modification.
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年学术文章
@wuu
2005年学术文章
@zh
2005年学术文章
@zh-cn
2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
@zh-sg
2005年學術文章
@yue
2005年學術文章
@zh-hant
name
Aziridine-2-carboxylic acid-co ...... elective peptide modification.
@en
Aziridine-2-carboxylic acid-co ...... elective peptide modification.
@nl
type
label
Aziridine-2-carboxylic acid-co ...... elective peptide modification.
@en
Aziridine-2-carboxylic acid-co ...... elective peptide modification.
@nl
prefLabel
Aziridine-2-carboxylic acid-co ...... elective peptide modification.
@en
Aziridine-2-carboxylic acid-co ...... elective peptide modification.
@nl
P2093
P356
P1476
Aziridine-2-carboxylic acid-co ...... elective peptide modification.
@en
P2093
Danica P Galonić
David Y Gin
Nathan D Ide
P304
P356
10.1021/JA050304R
P407
P577
2005-05-01T00:00:00Z