about
Total synthesis of glycosylated proteinsChemical and semisynthesis of posttranslationally modified proteins.The winding pathway to erythropoietin along the chemistry-biology frontier: a success at last.Toward Homogeneous Erythropoietin: Application of Metal Free Dethiylation in the Chemical Synthesis of the Ala79-Arg166 Glycopeptide Domain.Prospects in the total synthesis of protein therapeutics.Synthetic cysteine surrogates used in native chemical ligation.Patchwork protein chemistry: a practitioner's treatise on the advances in synthetic peptide stitchery.Peptide ligation chemistry at selenol amino acids.Developments and recent advancements in the field of endogenous amino acid selective bond forming reactions for bioconjugation.Oxidative Deselenization of Selenocysteine: Applications for Programmed Ligation at Serine.At last: erythropoietin as a single glycoformProbing the frontiers of glycoprotein synthesis: the fully elaborated β-subunit of the human follicle-stimulating hormone.Engineering of therapeutic polypeptides through chemical synthesis: early lessons from human parathyroid hormone and analogues.Chemistry as an expanding resource in protein science: fully synthetic and fully active human parathyroid hormone-related protein (1-141).Advances in proline ligation.Proline editing: a general and practical approach to the synthesis of functionally and structurally diverse peptides. Analysis of steric versus stereoelectronic effects of 4-substituted prolines on conformation within peptides.Peptide ligation-desulfurization chemistry at arginine.Chemoselective peptide ligation-desulfurization at aspartate.A molecular engineering toolbox for the structural biologist.Thirteen decades of peptide synthesis: key developments in solid phase peptide synthesis and amide bond formation utilized in peptide ligation.Synthesis of human growth hormone-releasing hormone via three-fragment serine/threonine ligation (STL).Aziridine-Mediated Ligation at Phenylalanine and Tryptophan Sites.Traceless reductive ligation at a tryptophan site: a facile access to β-hydroxytryptophan appended peptides.Synthesis of l- and d-Ubiquitin by One-Pot Ligation and Metal-Free Desulfurization.The phenacyl group as an efficient thiol protecting group in a peptide condensation reaction by the thioester method.Traceless β-mercaptan-assisted activation of valinyl benzimidazolinones in peptide ligations.A Type of Auxiliary for Native Chemical Peptide Ligation beyond Cysteine and Glycine Junctions.Synthesis of Poly-Ubiquitin Chains Using a Bifunctional Ubiquitin Monomer.
P2860
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P2860
description
2011 nî lūn-bûn
@nan
2011 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
An advance in proline ligation.
@ast
An advance in proline ligation.
@en
type
label
An advance in proline ligation.
@ast
An advance in proline ligation.
@en
prefLabel
An advance in proline ligation.
@ast
An advance in proline ligation.
@en
P2093
P2860
P356
P1476
An advance in proline ligation.
@en
P2093
Samuel J Danishefsky
Shiying Shang
Suwei Dong
Zhongping Tan
P2860
P304
10784-10786
P356
10.1021/JA204277B
P407
P577
2011-06-23T00:00:00Z