Iminoboronates: A New Strategy for Reversible Protein Modification
about
Click chemistry in complex mixtures: bioorthogonal bioconjugationFast and Tight Boronate Formation for Click Bioorthogonal Conjugation.Fabricating Triple-Sensitive Polymer Nano-Aggregates via an Aqueous Iminoboronate Multicomponent Reaction.Simultaneous construction of two linkages for the on-surface synthesis of imine-boroxine hybrid covalent organic frameworksDirect arginine modification in native peptides and application to chemical probe development.Targeting bacteria via iminoboronate chemistry of amine-presenting lipids.Iminoboronate-Based Peptide Cyclization That Responds to pH, Oxidation, and Small Molecule Modulators.Click with a boronic acid handle: a neighboring group-assisted click reaction that allows ready secondary functionalization.Iminoboronate Formation Leads to Fast and Reversible Conjugation Chemistry of α-Nucleophiles at Neutral pH.Fast and selective labeling of N-terminal cysteines at neutral pH via thiazolidino boronate formation.Functional systems with orthogonal dynamic covalent bonds.Smart chemistry in polymeric nanomedicine.Lysine-Targeting Covalent Inhibitors.Reversible lysine modification on proteins by using functionalized boronic acids.Targeted Covalent Inhibitors for Drug Design.Targeting biomolecules with reversible covalent chemistryComparison of boron-assisted oxime and hydrazone formations leads to the discovery of a fluorogenic variant.Rapid formation of a stable boron-nitrogen heterocycle in dilute, neutral aqueous solution for bioorthogonal coupling reactions.Residue-Specific Peptide Modification: A Chemist's Guide.Targeting cancer cells with folic acid-iminoboronate fluorescent conjugates.Boronic acids facilitate rapid oxime condensations at neutral pH.Arylboronic acid chemistry under electrospray conditions.'Borono-lectin' based engineering as a versatile platform for biomedical applications.The versatility of boron in biological target engagement.Dynamic Covalent Chemistry within Biphenyl Scaffolds: Reversible Covalent Bonding, Control of Selectivity, and Chirality Sensing with a Single System.Formation of hydrazones and stabilized boron-nitrogen heterocycles in aqueous solution from carbohydrazides and ortho-formylphenylboronic acids.Inhibition of Mcl-1 through covalent modification of a noncatalytic lysine side chain.Imine-based [2]catenanes in water.Palladium-Mediated Arylation of Lysine in Unprotected Peptides.Rapid labelling and covalent inhibition of intracellular native proteins using ligand-directed N-acyl-N-alkyl sulfonamide.Aryl transition metal chemical warheads for protein bioconjugationA Three-Component Assembly Promoted by Boronic Acids Delivers a Modular Fluorophore Platform (BASHY Dyes)Boron-Nitrogen BondIminoboronates are efficient intermediates for selective, rapid and reversible -terminal cysteine functionalisationDiscovery of new heterocycles with activity against human neutrophile elastase based on a boron promoted one-pot assembly reaction
P2860
Q26828895-F68C0D19-1FB8-413D-9735-05E64FAE5B0FQ31049089-C45CB163-2A88-48FB-9CCE-F7EC5C01F3D9Q31163867-1FA6566C-D8A1-4D86-B991-A4BBF5D373C3Q33609639-54379451-2B75-4948-BB1F-907F66AEEEEDQ34699009-BC3BD7F1-206D-4BFB-8195-55C681D6F3F1Q35186346-21AD0026-6D5C-491F-BE7D-8170869643EAQ35917996-38469EF8-1931-4389-90FD-875950A9001FQ36154919-A6F00568-5512-4206-861D-B1D338080678Q36425546-D6BF332A-2E9D-4FE7-A032-A40035803810Q37546173-5DB876D3-6913-4CA1-B5BE-B7043ED09149Q38167252-7674D981-F356-41A4-839C-945F09528DFBQ38221776-C9466C5B-D070-4FC5-92C8-9324901E1F5AQ38635726-C68A6490-1021-44A1-811E-12B8D6180F07Q38883755-20320081-EB17-49A6-833C-ABA756F0595AQ38931379-4E8B9BF4-A99A-4B0C-BD52-36DF1E16AF87Q38947282-7F41AAB6-F881-4D25-A8DD-9FA9517456A7Q39997356-8DB1BD2F-13B0-40C5-B52F-E483ADD34689Q43165833-6B762949-058C-4660-BAD1-4936B7DFBD2DQ43905157-92C7D288-00D5-41B7-B6B6-BAA401BEE0C4Q44588616-9C20B3C1-3176-4E73-BA30-8CEAA08EA8C8Q44899886-5DA9F0A0-4096-4850-A1AE-57FD3A7D665CQ45733270-F17430C3-21CF-4C59-A469-D9E909979E0DQ47131624-8679C7C0-0EA2-4EC7-96CA-A7F30D6C7E81Q48014676-9821A777-A546-4F14-A5B5-4B7E1B9FA225Q48119873-C5629744-B00A-4179-A138-ED8BD40C779BQ50275640-5BB349EB-0C06-4A51-ACC1-E60F04F96B24Q51533605-CBAAFAA4-9E36-44AE-9335-7433C5277DDCQ52314836-D1B53F13-A256-485E-867B-D90FB012C5D9Q52720422-3A439F5D-E3FF-49ED-96E3-4823FED29785Q55318660-93B13F38-C483-46EF-9E97-7240DF7BD270Q57776704-9FAE4679-94D4-4A8F-BA8C-5BF29ADD0420Q57976124-711CD4CC-9A23-43F0-945C-D29D8DD4F9A6Q57976127-5D854081-8F0B-4651-8E67-0B82CB14B6A7Q57976137-61200D3E-D33F-464F-9716-7B224A291589Q57976161-BC88E026-33B5-40AC-A9EB-2F7B9D783D72
P2860
Iminoboronates: A New Strategy for Reversible Protein Modification
description
im Juni 2012 veröffentlichter wissenschaftlicher Artikel
@de
scientific article published on 11 June 2012
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована в червні 2012
@uk
name
Iminoboronates: A New Strategy for Reversible Protein Modification
@en
Iminoboronates: A New Strategy for Reversible Protein Modification
@nl
type
label
Iminoboronates: A New Strategy for Reversible Protein Modification
@en
Iminoboronates: A New Strategy for Reversible Protein Modification
@nl
prefLabel
Iminoboronates: A New Strategy for Reversible Protein Modification
@en
Iminoboronates: A New Strategy for Reversible Protein Modification
@nl
P50
P356
P1476
Iminoboronates: a new strategy for reversible protein modification
@en
P2093
Elisabete Pires
P304
10299-10305
P356
10.1021/JA303436Y
P407
P577
2012-06-11T00:00:00Z