about
Advances in Fmoc solid-phase peptide synthesisOptimized approaches for quantification of drug transporters in tissues and cells by MRM proteomicsAutomated solid-phase peptide synthesis to obtain therapeutic peptidesSynthesis of peptide radiopharmaceuticals for the therapy and diagnosis of tumor diseasesRemoval of the 5-nitro-2-pyridine-sulfenyl protecting group from selenocysteine and cysteine by ascorbolysisProtection ReactionsDesign of S-Allylcysteine in Situ Production and Incorporation Based on a Novel Pyrrolysyl-tRNA Synthetase Variant.Chemoselective Synthesis of Carbamates using CO2 as Carbon Source.Tetrahydropyranyl: A Non-aromatic, Mild-Acid-Labile Group for Hydroxyl Protection in Solid-Phase Peptide Synthesis.Understanding Tetrahydropyranyl as a Protecting Group in Peptide Chemistry.New insight on 2-naphthylmethyl (NAP) ether as a protecting group in carbohydrate synthesis: a divergent approach towards a high-mannose type oligosaccharide library.Metal-binding and redox properties of substituted linear and cyclic ATCUN motifs.Radiosyntheses using fluorine-18: the art and science of late stage fluorinationCopper-peptide complex structure and reactivity when found in conserved His-X(aa)-His sequencesCharged or aromatic anchor residue dependence of transmembrane peptide tilt.Template-directed synthesis in 3'- and 5'-direction with reversible termination.Expanding the scope of PNA-encoded synthesis (PES): Mtt-protected PNA fully orthogonal to fmoc chemistry and a broad array of robust diversity-generating reactions.mRNA display selection and solid-phase synthesis of Fc-binding cyclic peptide affinity ligands.Synthesis and characterisation of self-assembled and self-adjuvanting asymmetric multi-epitope lipopeptides of ovalbumin.A simple protocol for combinatorial cyclic depsipeptide libraries sequencing by matrix-assisted laser desorption/ionisation mass spectrometry.Ru-catalysed C-H arylation of indoles and pyrroles with boronic acids: scope and mechanistic studiesShifting Native Chemical Ligation into Reverse through N→S Acyl Transfer.2,2'-Dithiobis(5-nitropyridine) (DTNP) as an effective and gentle deprotectant for common cysteine protecting groups.The use of 2,2'-dithiobis(5-nitropyridine) (DTNP) for deprotection and diselenide formation in protected selenocysteine-containing peptides.C-terminal peptide extension via gas-phase ion/ion reactions.Extra- and intracellular imaging of human matrix metalloprotease 11 (hMMP-11) with a cell-penetrating FRET substrate.Chemoenzymatic Synthesis of Acyl Coenzyme A Substrates Enables in Situ Labeling of Small Molecules and Proteins.Chemical synthesis, backbone cyclization and oxidative folding of cystine-knot peptides: promising scaffolds for applications in drug design.Self-assembly in nature: using the principles of nature to create complex nanobiomaterials."Click" reactions: a versatile toolbox for the synthesis of peptide-conjugates.Drug delivery and release systems for targeted tumor therapy.Review backbone N-modified peptides: How to meet the challenge of secondary amine acylation.Flexibility is important for inhibition of the MDM2/p53 protein-protein interaction by cyclic β-hairpins.Chemical Synthesis of Antimicrobial Peptides.A modified Tat peptide for selective intracellular delivery of macromolecules.Halogen Bonding: A Powerful Tool for Modulation of Peptide Conformation.GAP Peptide Synthesis via Design of New GAP Protecting Group: An Fmoc/tBu Synthesis of Thymopentin Free from Polymers, Chromatography and Recrystallization.Total synthesis and structure-activity relationship studies of a series of selective G protein inhibitors.Efficient generation of peptide hydrazides via direct hydrazinolysis of Peptidyl-Wang-TentaGel resins.Synthesis of a HyCoSuL peptide substrate library to dissect protease substrate specificity.
P2860
Q26770921-F0BA5395-3F34-4C5E-A199-216420598463Q26851693-E4652399-D2FA-4ECC-8312-97DA8B3ED705Q27001623-192C6A4A-25D8-40E9-A225-BCF43FCE6A10Q27025187-C62CF747-BDD9-407E-A39B-AC01E693F301Q28821989-EEF5B912-2808-4E58-8AB8-91383775F77DQ30048980-60854A0E-F963-42BE-9FC8-5B5C1F37E238Q30395377-512B0341-1312-4BB1-8304-09BA4E1DC12AQ33468324-61565AF1-2387-44D2-8517-9C920D5D158DQ33562045-1EC19C0B-7E02-4EAD-B7F5-FE864FD05878Q33562072-B4CFEF28-9CB8-4982-95D5-76FEACC75BC0Q33953440-C29229EF-B63F-4B68-B02C-6D91CD263F34Q33993654-890F1A04-7C9C-4FE5-860F-A2B38C6E5F53Q34074437-A27948D2-161A-4037-8765-50AD820D7B0DQ34160472-AD8D3649-749D-4490-92ED-A01610ABB569Q34181541-89C9C119-FDCA-4AC4-B581-1E466395A791Q34331715-8A01B4BE-6B47-4D5E-AB4D-2A9794F9A122Q34390347-4E626F8E-2017-4AF9-855B-78CC1ED269C7Q34459997-F2F0B8CD-0D59-431C-AD63-96B8086F62F4Q35423378-9D35DDE5-7587-4E1D-9FF9-06A912F7A89EQ35446970-B1EE28BE-3E6A-4F32-90B6-1B7202480E57Q35562633-DEEA32F3-790A-417C-8F8B-84CC4A1BBC9AQ35752105-6308BA79-F665-453A-AECD-8F76ADDD8BD5Q35789260-6F9B5DB3-4141-45FC-AECD-6296032DD738Q36222347-A53E5F86-00EC-4159-B612-63E562E35D8DQ36338128-DD2D0817-E2F8-4A17-84A6-ACCA75745B1CQ36368221-77F837BE-3016-453D-B8FC-2E087D63BD81Q36482701-5DD0062B-B612-4015-8E72-5646FC41BCDBQ38055326-232DFC2C-2BCA-4B83-865C-7424C691669EQ38127659-027D83F3-6E1E-4254-9AB7-B21AF019A639Q38226023-6C6AF195-3A6C-4631-81A5-F91C549863AEQ38363691-0C01FDD9-7480-4AFA-9BCA-A09398811544Q38533393-86954A85-BB06-48E5-8495-42936F3BB07BQ38812479-CDC0A0DA-6094-40BA-825A-809149759C3CQ39053445-06B57EE8-7427-4314-B9DD-EB9CADA778C8Q39558788-EC431E9E-7D8D-43C0-B447-91D0BBD4C5A8Q41012447-521BC290-3F9F-43BC-9FCA-A7A2D4DF33FFQ41027969-A3C27AF5-F1E5-4932-92FE-D249548A3A35Q41438187-F7FEB012-85DD-4A9F-967A-8A211624BE10Q41483711-127B4185-CA1D-4A9C-96CF-53BE8F447BAEQ41933022-45967033-B666-4477-8EBF-0C991332819E
P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on June 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Amino acid-protecting groups.
@en
Amino acid-protecting groups.
@nl
type
label
Amino acid-protecting groups.
@en
Amino acid-protecting groups.
@nl
prefLabel
Amino acid-protecting groups.
@en
Amino acid-protecting groups.
@nl
P2093
P356
P1433
P1476
Amino acid-protecting groups.
@en
P2093
Albert Isidro-Llobet
Fernando Albericio
Mercedes Alvarez
P304
P356
10.1021/CR800323S
P577
2009-06-01T00:00:00Z