COMU: a safer and more effective replacement for benzotriazole-based uronium coupling reagents.
about
Dendrimers as tunable vectors of drug delivery systems and biomedical and ocular applicationsAutomated solid-phase peptide synthesis to obtain therapeutic peptidesGlobal shape and ligand binding efficiency of the HIV-1-neutralizing antibodies differ from those of antibodies that cannot neutralize HIV-1Screening of N-alkyl-cyanoacetamido oximes as substitutes for N-hydroxysuccinimideA green approach to the synthesis of novel phytosphingolipidyl β-cyclodextrin designed to interact with membranes.Effect of residual water and microwave heating on the half-life of the reagents and reactive intermediates in peptide synthesis.A fragment merging approach towards the development of small molecule inhibitors of Mycobacterium tuberculosis EthR for use as ethionamide boostersOptimization of adenosine 5'-carboxamide derivatives as adenosine receptor agonists using structure-based ligand design and fragment screening.G-protein signaling leverages subunit-dependent membrane affinity to differentially control βγ translocation to intracellular membranes.Evaluation of High-Yield Purification Methods on Monodisperse PEG-Grafted Iron Oxide Nanoparticles.Synthesis and characterisation of PEG-peptide surfaces for proteolytic enzyme detectionMicrowave heating in solid-phase peptide synthesis.COMU: scope and limitations of the latest innovation in peptide acyl transfer reagents.Cu-mediated enamide formation in the total synthesis of complex peptide natural products.An update on new methods to synthesize cyclotetrapeptides.Mycothiol synthesis by an anomerization reaction through endocyclic cleavage.Chemical Synthesis of Antimicrobial Peptides.Monoenomycin: A Simplified Trienomycin A Analogue that Manifests Anticancer Activity.The total synthesis and functional evaluation of fourteen stereoisomers of yaku'amide B. The importance of stereochemistry for hydrophobicity and cytotoxicity.Total Synthesis of Mycobacterium tuberculosis Dideoxymycobactin-838 and Stereoisomers: Diverse CD1a-Restricted T Cells Display a Common Hierarchy of Lipopeptide Recognition.Interface Immobilization Chemistry of cRGD-based Peptides Regulates Integrin Mediated Cell Adhesion.Isolation and Synthesis of Laxaphycin B-Type Peptides: A Case Study and Clues to Their Biosynthesis.(2S,4R)- and (2S,4S)-perfluoro-tert-butyl 4-hydroxyproline: two conformationally distinct proline amino acids for sensitive application in 19F NMR.Synthesis and activity of a novel inhibitor of nonsense-mediated mRNA decayIndividually Stabilized, Superparamagnetic Nanoparticles with Controlled Shell and Size Leading to Exceptional Stealth Properties and High Relaxivities.Complete Exchange of the Hydrophobic Dispersant Shell on Monodisperse Superparamagnetic Iron Oxide Nanoparticles.Stereocontrolled syntheses of peptide thioesters containing modified seryl residues as probes of antibiotic biosynthesis.Synthesis of cruentaren ABOP-OXy, BOP-OBt, and BOP-OAt: novel organophosphinic coupling reagents useful for solution and solid-phase peptide synthesis.Heating and microwave assisted SPPS of C-terminal acid peptides on trityl resin: the truth behind the yield.Mechanistic insight into benzenethiol catalyzed amide bond formations from thioesters and primary amines.Efficient α-helix induction in a linear peptide chain by N-capping with a bridged-tricyclic diproline analogue.Oxyma-B, an excellent racemization suppressor for peptide synthesis.TOMBU and COMBU as Novel Uronium-type peptide coupling reagents derived from Oxyma-B.Re-evaluating the stability of COMU in different solvents.Direct N-alkylation of unprotected amino acids with alcohols.Target Identification and Mechanism of Action of Picolinamide and Benzamide Chemotypes with Antifungal Properties.Towards the Shell Biorefinery: Sustainable Synthesis of the Anticancer Alkaloid Proximicin A from Chitin.Thirteen decades of peptide synthesis: key developments in solid phase peptide synthesis and amide bond formation utilized in peptide ligation.Stereoselective synthesis of Arabidopsis CLAVATA3 (CLV3) glycopeptide, unique protein post-translational modifications of secreted peptide hormone in plant.
P2860
Q26771189-5BA9143C-6BFE-48FD-85D4-A8EB10880CF3Q27001623-F4D5064B-480F-4E07-A6BE-3653550B02F5Q28250040-4A9EE8C3-10FE-4552-A3BF-3BD50CF47C7EQ30760023-D4FB8294-623F-4E19-BA67-8760B1A67082Q30882375-4018E8FF-3A4D-4A62-B4C9-141D5E14C32FQ34303754-E6AFD35E-D766-40D2-9305-3D040E86ABD5Q35902882-0349F464-B890-4596-B0ED-3D40AE044258Q36343219-3B3C92AB-C946-47DA-ACCF-DB95344C330CQ36485377-8A1534B0-5536-4104-9DDD-0F6026A669F8Q36904750-4A3C6AD6-324C-4BE1-9A75-DDE6D811F85CQ37302361-8573E41A-508E-4483-BCA1-39C0851B7BA8Q37947476-0C354877-B242-4B6F-91B9-46F462D9908CQ38109879-1276E3C0-76B6-42BB-B64D-B19155206EE9Q38190893-4D1B3110-69E6-49CB-90EF-7B8F0EEC1DDDQ38506994-FF679BD0-D0F9-4057-A9CD-6954206DE530Q38781699-F35508CF-F801-4F8F-992A-3602BAF258E4Q39053445-E3F6E900-5F6E-45BE-A0E3-1FEF1162770BQ39586528-52B8E181-3D13-43E7-9E9B-7C7007EC37F0Q39832057-897274DB-CEB1-4DCD-BF0B-5100384D1280Q40420706-1120A186-FFC2-48F9-AD07-9F8F91B5DE24Q41157466-B8430401-1282-4420-A5F3-917543273A8AQ41323194-AFF1C3C3-5786-4409-9F2E-208C169F2219Q41515173-45EEA5A5-A16D-4EA6-827F-2D6D56D8DEF0Q41766492-3B14B9D4-7B8A-46E7-8508-837D5109245AQ41846933-62EB9034-F0FB-4C9B-9F01-137CA64D3EFBQ41863235-38A153F3-880E-4AF7-BF3A-F83240784DB3Q41885234-5B87FD76-B205-4740-B631-907B75FAFCA3Q42118014-2CC64B3D-C2FB-47C6-9813-4B3FA28DC9C3Q43963007-0A0A23EA-4A34-46C4-BC0E-3296C52DF58BQ44705983-3092F06F-53A5-477A-8452-2354E68FCAD2Q46081185-A9E158EB-4FD0-48AA-B138-ECFBF915CA9BQ46468024-EF688E71-5132-4815-9488-389019AF368FQ46496942-0A15B4FA-DA62-423C-9245-47EE8266BBA9Q46614316-68068128-7155-4E8D-B2E4-77B9416C2ABCQ46911002-AEDD2D1A-4D84-4CE4-B52E-FB19C9B3C7A0Q47094747-AA7D7024-09A1-444E-8E4F-17F86D804B47Q47226064-CF1DCEA1-193B-49F6-B22B-C7202D217124Q47244276-ED27192A-0D35-4BF4-A602-809564269BF2Q47353754-04AB63BF-F404-4B56-B3FD-15D952FA5D0DQ47867252-46D0FA53-6585-4E24-8815-1D5DB4126D62
P2860
COMU: a safer and more effective replacement for benzotriazole-based uronium coupling reagents.
description
2009 nî lūn-bûn
@nan
2009 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
COMU: a safer and more effecti ...... sed uronium coupling reagents.
@ast
COMU: a safer and more effecti ...... sed uronium coupling reagents.
@en
type
label
COMU: a safer and more effecti ...... sed uronium coupling reagents.
@ast
COMU: a safer and more effecti ...... sed uronium coupling reagents.
@en
prefLabel
COMU: a safer and more effecti ...... sed uronium coupling reagents.
@ast
COMU: a safer and more effecti ...... sed uronium coupling reagents.
@en
P50
P356
P1476
COMU: a safer and more effecti ...... sed uronium coupling reagents.
@en
P2093
Ramon Subirós Funosas
P304
P356
10.1002/CHEM.200900615
P407
P577
2009-09-01T00:00:00Z