About: Studies Related to the Relative Thermodynamic Stability of C-Terminal Peptidyl Esters of O-Hydroxy Thiophenol: Emergence of a Doable Strategy for Non-Cysteine Ligation Applicable to the Chemical Synthesis of Glycopeptides

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About: Studies Related to the Relative Thermodynamic Stability of C-Terminal Peptidyl Esters of O-Hydroxy Thiophenol: Emergence of a Doable Strategy for Non-Cysteine Ligation Applicable to the Chemical Synthesis of Glycopeptides Goto Sponge Distinct Permalink

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scientific article published on 01 June 2006

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в червні 2006 (uk) im Juni 2006 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en xunu de 2006 (ast) scientific article published on 01 June 2006 (en)
publication date	wds:Q58322746-E5DF88E3-019C-4E7C-B808-CFB6A9A31BC5
publication date	2006-06-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q58322746-60D35715-96E2-4CF7-8798-09E92874988E
language of work or name	English
author name string	wds:Q58322746-158D0EDA-EBAB-47BA-AA8D-0F280323E337 wds:Q58322746-177766A4-EA23-4326-8280-F902A8FBA7A4 wds:Q58322746-51CCB407-22E8-41A6-83E9-5278D0AD3A9C wds:Q58322746-DB846233-860E-4371-846B-BBDE88C2BCEB
author name string	Gong Chen Bin Wu Samuel J Danishefsky Jiehao Chen
rdfs:label	Studies Related to the Relative Thermodynamic Stability of C-Terminal Peptidyl Esters of O-Hydroxy Thiophenol: Emergence of a Doable Strategy for Non-Cysteine Ligation Applicable to the Chemical Synthesis of Glycopeptides (en) Studies Related to the Relative Thermodynamic Stability of C-Terminal Peptidyl Esters of O-Hydroxy Thiophenol: Emergence of a Doable Strategy for Non-Cysteine Ligation Applicable to the Chemical Synthesis of Glycopeptides (nl)
skos:prefLabel	Studies Related to the Relative Thermodynamic Stability of C-Terminal Peptidyl Esters of O-Hydroxy Thiophenol: Emergence of a Doable Strategy for Non-Cysteine Ligation Applicable to the Chemical Synthesis of Glycopeptides (en) Studies Related to the Relative Thermodynamic Stability of C-Terminal Peptidyl Esters of O-Hydroxy Thiophenol: Emergence of a Doable Strategy for Non-Cysteine Ligation Applicable to the Chemical Synthesis of Glycopeptides (nl)
name	Studies Related to the Relative Thermodynamic Stability of C-Terminal Peptidyl Esters of O-Hydroxy Thiophenol: Emergence of a Doable Strategy for Non-Cysteine Ligation Applicable to the Chemical Synthesis of Glycopeptides (en) Studies Related to the Relative Thermodynamic Stability of C-Terminal Peptidyl Esters of O-Hydroxy Thiophenol: Emergence of a Doable Strategy for Non-Cysteine Ligation Applicable to the Chemical Synthesis of Glycopeptides (nl)
author	wds:Q58322746-470E5D0B-35A6-4E28-B692-4E20601BB6A0 wds:Q58322746-607BE500-CFC1-4698-843C-7FF5E78FA9F2
author	Qian Wan J David Warren
title	wds:Q58322746-5548CE72-3A5E-4DDE-864A-B03ECCCCB7B5
title	Studies related to the relative thermodynamic stability of C-terminal peptidyl esters of O-hydroxy thiophenol: emergence of a doable strategy for non-cysteine ligation applicable to the chemical synthesis of glycopeptides (en)
page(s)	wds:Q58322746-11733628-E3B5-4B9F-AD80-5BD306E45444
page(s)	7460-7462
instance of	wds:Q58322746-CE9705BA-0229-4129-87E4-4B949A34858C
instance of	scholarly article
PubMed ID	wds:Q58322746-C685F854-9CA9-4AB4-BA56-1227276B48D3
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/16756298
PubMed ID	16756298
published in	wds:Q58322746-C1EAA94E-E3A3-4D1C-98C5-79D95D6C68B9
published in	Journal of the American Chemical Society
issue	wds:Q58322746-AEED453D-ADD0-4BDA-8D71-4B9EEB70F713
volume	wds:Q58322746-A2DD8292-A01B-4A89-A5EB-7C45B68D9070
issue	23
volume	128
DOI	wds:Q58322746-B2B75B79-378C-449D-A52D-D34EC70F624D
DOI	http://dx.doi.org/10.1021/JA061588Y
DOI	10.1021/JA061588Y
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q58322746
is cites work of	Toward homogeneous erythropoietin: fine tuning of the C-terminal acyl donor in the chemical synthesis of the Cys29-Gly77 glycopeptide domain Mature Homogeneous Erythropoietin-Level Building Blocks by Chemical Synthesis: The EPO 114-166 Glycopeptide Domain, Presenting the O-Linked Glycophorin Native chemical ligation at valine: a contribution to peptide and glycopeptide synthesis. Toward homogeneous erythropoietin: non-NCL-based chemical synthesis of the Gln78-Arg166 glycopeptide domain Erythropoietin derived by chemical synthesis Functional and mechanistic analyses of biomimetic aminoacyl transfer reactions in de novo designed coiled coil peptides via rational active site engineering. Biomimetic catalysis of intermodular aminoacyl transfer The winding pathway to erythropoietin along the chemistry-biology frontier: a success at last. Native chemical ligation of thioamide-containing peptides: development and application to the synthesis of labeled α-synuclein for misfolding studies At last: erythropoietin as a single glycoform Shifting Native Chemical Ligation into Reverse through N→S Acyl Transfer Internal Cysteine Accelerates Thioester-Based Peptide Ligation Sugar-assisted glycopeptide ligation with complex oligosaccharides: scope and limitations Toward fully synthetic, homogeneous glycoproteins: advances in chemical ligation. Protein chemical synthesis by serine and threonine ligation Revisiting oxytocin through the medium of isonitriles An advance in proline ligation Oxo-ester mediated native chemical ligation: concept and applications. Chemical synthesis of membrane proteins: a model study on the influenza virus B proton channel. Recent Departures in the Synthesis of Peptides and Glycopeptides The C-Terminal O-S Acyl Shift Pathway under Acidic Condition to Propose Peptide-Thioesters. Synthesis of glycopeptides. Biomimetic catalysis of diketopiperazine and dipeptide syntheses. Preparation of Peptide Thioesters through Fmoc-Based Solid-Phase Peptide Synthesis by Using Amino Thioesters
is cites work of	wds:Q33938752-DB7B0BC6-1481-4ADE-9BFA-6DD72DE68EB6 wds:Q35752105-2D352432-C8D6-4FB0-ADB1-5EFF0EADE983 wds:Q43247324-A0BC04FA-07E6-4847-AB4C-158DAA654F17 wds:Q58001641-F57135DC-DFC3-42B4-96A4-9D3DC6E63823 wds:Q33840717-55F06B6B-B963-4ABA-AD7F-63A229B32AE1 wds:Q37395648-7E70A2FE-5C1A-49F9-8DCF-4A426C1D6D1A wds:Q37428099-D4DF4F18-62A0-464C-B1BB-1C79FF619D03 wds:Q52714587-D123F088-ABF6-4EB4-A79B-5F2A0516FAFF wds:Q42034117-DF942FCF-C831-41D8-8BF0-9A58A74E64B3 wds:Q53670284-DE7864F0-E93E-4225-BDF0-AD7DA88B3D25 wds:Q37373969-E2648531-7650-4448-AE95-16DAC1605F4A wds:Q37104945-4599D914-3902-4AC4-A8E0-6C5AC367253C wds:Q36153110-386A2C18-70A8-43C4-9B3E-D1FDA7C9110F wds:Q39923486-47940885-39D2-442B-B9B9-DD5F478962A6 wds:Q39923516-0B54DE38-E270-4AA7-91AA-1BB37A8F7706 wds:Q58377366-6902CD03-2C78-497C-AE2A-2BA6D95A7BB1 wds:Q42162157-889A8FF9-9BFE-4E71-819F-C585A47B4711 wds:Q35103688-EE322E2A-BFE0-48E6-ACAF-ECBDF4CE4FDC wds:Q41439313-637382D5-EC15-48DB-92D8-FD2E125F878D wds:Q36508946-478BC590-C1CD-44EA-AA53-2EB1DE34FF1D wds:Q36799143-182191E5-23BD-4141-B076-94E320F249E9 wds:Q37769179-2B50F13C-81CC-4AB0-88DB-6E19D31CF5E1 wds:Q42123499-47D38D8E-0666-4E42-B329-37072BB37135 wds:Q44947276-9FB047B3-602D-4D93-BA34-DC1B8FF98C60

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