On the public citation graph
Heterocyclic Peptide Backbone Modifications in an α-Helical Coiled Coil
0 signed · 492 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/1097-0282(2001)60:3<194::aid-bip10031>3.0.co;2-8openalex-snapshot
Methods and strategies of peptide ligation
inferredcites →https://doi.org/10.1002/1521-3773(20020715)41:14<2596::aid-anie2596>3.0.co;2-4openalex-snapshot
A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective “Ligation” of Azides and Terminal Alkynes
inferredcites →https://doi.org/10.1002/1521-3773(20020715)41:14<2599::aid-anie2599>3.0.co;2-nopenalex-snapshot
Electronic and Steric Effects on Catalysts for CO2/Epoxide Polymerization: Subtle Modifications Resulting in Superior Activities
inferredcites →https://doi.org/10.1006/jmbi.1995.0492openalex-snapshot
The Occurence of C–H · · · O Hydrogen Bonds in Proteins
inferredcites →https://doi.org/10.1021/ja001648eopenalex-snapshot
Design, Synthesis, and Characterization of 4-Ester CI2, a Model for Backbone Hydrogen Bonding in Protein α-Helices
inferredcites →https://doi.org/10.1021/ja010775nopenalex-snapshot
The Energetic Contribution of Backbone−Backbone Hydrogen Bonds to the Thermodynamic Stability of a Hyperstable P22 Arc Repressor Mutant
inferredcites →https://doi.org/10.1021/ja020887uopenalex-snapshot
Synthesis of Sugar Arrays in Microtiter Plate
inferredcites →https://doi.org/10.1021/ja021381eopenalex-snapshot
Bioconjugation by Copper(I)-Catalyzed Azide-Alkyne [3 + 2] Cycloaddition
inferredcites →https://doi.org/10.1021/ja034490hopenalex-snapshot
Activity-Based Protein Profiling in Vivo Using a Copper(I)-Catalyzed Azide-Alkyne [3 + 2] Cycloaddition
inferredcites →https://doi.org/10.1021/ja036765zopenalex-snapshot
Cell Surface Labeling of Escherichia coli via Copper(I)-Catalyzed [3+2] Cycloaddition
inferredcites →https://doi.org/10.1021/ja0370037openalex-snapshot
Adding Amino Acids with Novel Reactivity to the Genetic Code of Saccharomyces Cerevisiae
inferredcites →https://doi.org/10.1021/ja970826+openalex-snapshot
Mutational Analysis of Backbone Hydrogen Bonds in Staphylococcal Nuclease
inferredcites →https://doi.org/10.1021/jo011148jopenalex-snapshot
Peptidotriazoles on Solid Phase: [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides
inferredcites →https://doi.org/10.1038/nature02478openalex-snapshot
Correction: Corrigendum: Global-scale temperature patterns and climate forcing over the past six centuries
inferredcites →https://doi.org/10.1038/nature02611openalex-snapshot
Context-dependent contributions of backbone hydrogen bonding to β-sheet folding energetics
inferredcites →https://doi.org/10.1126/science.8248779openalex-snapshot
A Switch Between Two-, Three-, and Four-stranded Coiled Coils in GCN4 Leucine Zipper Mutants
inferredcites →https://doi.org/10.1126/science.8248780openalex-snapshot
A Third Recognition Element in Bacterial Promoters: DNA Binding by the α Subunit of RNA Polymerase
inferredcites →https://doi.org/10.2174/1389557023405828openalex-snapshot
Peptidomimetics and Peptide Backbone Modifications
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4764327openalex-extracted
Design, Synthesis and Biological Evaluation of 1,2,3-Triazole Incorporated 1,2,4-Thiadiazole Fused Benzofuran Derivatives as Anticancer Agents
inferred← citeshttps://doi.org/10.2139/ssrn.4781047openalex-extracted
Study on Interaction with High-Abundant Blood Proteins and Identification of Low-Abundant Proteins to 5-Phenyl-1-(P-Tolyl)-1h-1,2,3-Triazole by Serum Proteomics
inferred← citeshttps://doi.org/10.2139/ssrn.4804411openalex-extracted
Study on Interaction with High-Abundant Blood Proteins and Identification of Low-Abundant Proteins to 5-Phenyl-1-(P-Tolyl)-1h-1,2,3-Triazole by Serum Proteomics
inferred← citeshttps://doi.org/10.1002/0471140864.ps1808s50openalex-snapshot
Overview of Solid Phase Synthesis of “Difficult Peptide” Sequences
inferred← citeshttps://doi.org/10.1002/0471440264.pst565openalex-snapshot
“Click” Chemistry in Macromolecular Synthesis
inferred← citeshttps://doi.org/10.1002/0471440264.pst663openalex-snapshot
Injectable Hydrogels: Properties and Applications
inferred← citeshttps://doi.org/10.1002/9780470661345.smc062openalex-snapshot
Anion Receptors Containing Heterocyclic Rings
inferred← citeshttps://doi.org/10.1002/9780470661345.smc156openalex-snapshot
Supramolecular Organocatalysis
inferred← citeshttps://doi.org/10.1002/9780470682517.ch10openalex-snapshot
Dipolar Cycloaddition Reactions in Peptide Chemistry
inferred← citeshttps://doi.org/10.1002/9780470748862.ch7openalex-snapshot
Click Chemistry on Supramolecular Materials
inferred← citeshttps://doi.org/10.1002/9781118526996.ch5openalex-snapshot
Clicking Sugars onto Sugars: Oligosaccharide Analogs and Glycoclusters on Carbohydrate Scaffolds
inferred← citeshttps://doi.org/10.1002/9781118683033.ch5openalex-snapshot
Click Chemistry: The Triazole Ring as a Privileged Peptidomimetic Scaffold
inferred← citeshttps://doi.org/10.1002/9781119044116.ch1openalex-snapshot
Introduction to Chemical Ligation Reactions
inferred← citeshttps://doi.org/10.1002/9783527343430.ch2openalex-snapshot
Construction of Constrained Helices
inferred← citeshttps://doi.org/10.1002/9783527631827.ch2openalex-snapshot
Huisgen Cycloaddition in Peptidomimetic Chemistry
inferred← citeshttps://doi.org/10.1002/9783527694174.ch1openalex-snapshot
Click Chemistry: Mechanistic and Synthetic Perspectives
inferred← citeshttps://doi.org/10.1002/9783527694174.ch5openalex-snapshot
Applications of the Cu ‐Catalyzed Azide–Alkyne Cycloaddition ( CuAAC ) in Peptides
inferred← citeshttps://doi.org/10.1002/adma.201305162openalex-snapshot
Click Chemistry Plays a Dual Role in Biodegradable Polymer Design
inferred← citeshttps://doi.org/10.1002/adsc.200404383openalex-snapshot
Click Chemistry: Copper Clusters Catalyse the Cycloaddition of Azides with Terminal Alkynes
inferred← citeshttps://doi.org/10.1002/adsc.200900353openalex-snapshot
Immobilization of Porphyrinatocopper Nanoparticles onto Activated Multi‐Walled Carbon Nanotubes and a Study of its Catalytic Activity as an Efficient Heterogeneous Catalyst for a Click Approach to the Three‐Component Synthesis of 1,2,3‐Triazoles in Water
inferred← citeshttps://doi.org/10.1002/adsc.201400904openalex-snapshot
Multicomponent Syntheses based upon Copper‐Catalyzed Alkyne‐Azide Cycloaddition
inferred← citeshttps://doi.org/10.1002/ajoc.201300245openalex-snapshot
Application of “Click” Chemistry to the Construction of Supramolecular Functional Systems
inferred← citeshttps://doi.org/10.1002/ange.200602248openalex-snapshot
Rational Design of Bioorganometallic Foldamers: A Potential Model for Parallel β‐Helical Peptides
inferred← citeshttps://doi.org/10.1002/ange.200704717openalex-snapshot
Pure CH Hydrogen Bonding to Chloride Ions: A Preorganized and Rigid Macrocyclic Receptor
inferred← citeshttps://doi.org/10.1002/ange.200801313openalex-snapshot
Chemoselektive Ligations‐ und Modifikationsstrategien für Peptide und Proteine
inferred← citeshttps://doi.org/10.1002/ange.200805009openalex-snapshot
Cycloaddition‐Promoted Self‐Assembly of a Polymer into Well‐Defined β Sheets and Hierarchical Nanofibrils
inferred← citeshttps://doi.org/10.1002/ange.200805900openalex-snapshot
Probing the Bioactive Conformation of an Archetypal Natural Product HDAC Inhibitor with Conformationally Homogeneous Triazole‐Modified Cyclic Tetrapeptides
inferred← citeshttps://doi.org/10.1002/ange.200805901openalex-snapshot
Conformationally Homogeneous Heterocyclic Pseudotetrapeptides as Three‐Dimensional Scaffolds for Rational Drug Design: Receptor‐Selective Somatostatin Analogues
inferred← citeshttps://doi.org/10.1002/ange.201008142openalex-snapshot
“Triazolbrücke”: ein Disulfidbrückenersatz durch Ruthenium‐ katalysierte Bildung von 1,5‐disubstituierten 1,2,3‐Triazolen
inferred← citeshttps://doi.org/10.1002/ange.201107222openalex-snapshot
Synthesis of a Biologically Active Triazole‐Containing Analogue of Cystatin A Through Successive Peptidomimetic Alkyne–Azide Ligations
inferred← citeshttps://doi.org/10.1002/ange.201303108openalex-snapshot
1,2,3‐Triazole als Mimetika der Amid‐Bindung: Ein Triazol‐Scan führt zu Protease‐resistenten Peptidmimetika für das Tumor‐Targeting
inferred← citeshttps://doi.org/10.1002/ange.201408265openalex-snapshot
Lewis Base Catalyzed Aerobic Oxidative Intermolecular Azide–Zwitterion Cycloaddition
inferred← citeshttps://doi.org/10.1002/ange.201707637openalex-snapshot
A De Novo Heterodimeric Due Ferri Protein Minimizes the Release of Reactive Intermediates in Dioxygen‐Dependent Oxidation
inferred← citeshttps://doi.org/10.1002/ange.202113129openalex-snapshot
Secondary Structure Tuning of a Pseudoprotein Between β‐Meander and α‐Helical Forms in the Solid‐State
inferred← citeshttps://doi.org/10.1002/ange.9299244openalex-snapshot
Azole γ‐Peptides Helix Switching via Heterocycle Substitutions
inferred← citeshttps://doi.org/10.1002/anie.200602248openalex-snapshot
Rational Design of Bioorganometallic Foldamers: A Potential Model for Parallel β‐Helical Peptides
inferred← citeshttps://doi.org/10.1002/anie.200704717openalex-snapshot
Pure CH Hydrogen Bonding to Chloride Ions: A Preorganized and Rigid Macrocyclic Receptor
inferred← citeshttps://doi.org/10.1002/anie.200801313openalex-snapshot
Chemoselective Ligation and Modification Strategies for Peptides and Proteins
inferred← citeshttps://doi.org/10.1002/anie.200805009openalex-snapshot
Cycloaddition‐Promoted Self‐Assembly of a Polymer into Well‐Defined β Sheets and Hierarchical Nanofibrils
inferred← citeshttps://doi.org/10.1002/anie.200805900openalex-snapshot
Probing the Bioactive Conformation of an Archetypal Natural Product HDAC Inhibitor with Conformationally Homogeneous Triazole‐Modified Cyclic Tetrapeptides
inferred← citeshttps://doi.org/10.1002/anie.200805901openalex-snapshot
Conformationally Homogeneous Heterocyclic Pseudotetrapeptides as Three‐Dimensional Scaffolds for Rational Drug Design: Receptor‐Selective Somatostatin Analogues
inferred← citeshttps://doi.org/10.1002/anie.201008142openalex-snapshot
“Triazole Bridge”: Disulfide‐Bond Replacement by Ruthenium‐Catalyzed Formation of 1,5‐Disubstituted 1,2,3‐Triazoles
inferred← citeshttps://doi.org/10.1002/anie.201107222openalex-snapshot
Synthesis of a Biologically Active Triazole‐Containing Analogue of Cystatin A Through Successive Peptidomimetic Alkyne–Azide Ligations
inferred← citeshttps://doi.org/10.1002/anie.201303108openalex-snapshot
1,2,3‐Triazoles as Amide Bond Mimics: Triazole Scan Yields Protease‐Resistant Peptidomimetics for Tumor Targeting
inferred← citeshttps://doi.org/10.1002/anie.201408265openalex-snapshot
Lewis Base Catalyzed Aerobic Oxidative Intermolecular Azide–Zwitterion Cycloaddition
inferred← citeshttps://doi.org/10.1002/anie.201707637openalex-snapshot
A De Novo Heterodimeric Due Ferri Protein Minimizes the Release of Reactive Intermediates in Dioxygen‐Dependent Oxidation
inferred← citeshttps://doi.org/10.1002/anie.202113129openalex-snapshot
Secondary Structure Tuning of a Pseudoprotein Between β‐Meander and α‐Helical Forms in the Solid‐State
inferred← citeshttps://doi.org/10.1002/anie.9299244openalex-snapshot
Azole γ‐Peptides Helix Switching via Heterocycle Substitutions
inferred← citeshttps://doi.org/10.1002/aoc.3398openalex-snapshot
Immobilized copper(II) on nitrogen‐rich polymer‐entrapped Fe 3 O 4 nanoparticles: a highly loaded and magnetically recoverable catalyst for aqueous click chemistry
inferred← citeshttps://doi.org/10.1002/app.31268openalex-snapshot
Functionalization of multi‐walled carbon nanotubes with poly(ε‐caprolactone) using click chemistry
inferred← citeshttps://doi.org/10.1002/asia.200700015openalex-snapshot
Triazole: the Keystone in Glycosylated Molecular Architectures Constructed by a Click Reaction
inferred← citeshttps://doi.org/10.1002/asia.201100329openalex-snapshot
Click to Join Peptides/Proteins Together
inferred← citeshttps://doi.org/10.1002/asia.201100378openalex-snapshot
Steroid/Triterpenoid Functional Molecules based on “Click Chemistry”
inferred← citeshttps://doi.org/10.1002/asia.201100432openalex-snapshot
Click Chemistry: 1,2,3‐Triazoles as Pharmacophores
inferred← citeshttps://doi.org/10.1002/asia.201901015openalex-snapshot
A General Proline‐Catalyzed Synthesis of 4,5‐Disubstituted N‐Sulfonyl‐1,2,3‐Triazoles from 1,3‐Dicarbonyl Compounds and Sulfonyl Azide
inferred← citeshttps://doi.org/10.1002/bip.22139openalex-snapshot
Solvent independent conformational propensities of [1,2,3]triazolyl‐bridged parathyroid hormone‐related peptide‐derived cyclo‐nonapeptide analogues
inferred← citeshttps://doi.org/10.1002/bip.22641openalex-snapshot
Straightforward strategy to substitute amide bonds by 1,2,3‐triazoles in peptaibols analogs using Aibψ[Tz]‐Xaa dipeptides
inferred← citeshttps://doi.org/10.1002/cbdv.200900013openalex-snapshot
Synthesis and Evaluation of Sphingolipid Analogues
inferred← citeshttps://doi.org/10.1002/cbdv.202402381openalex-snapshot
Design, Synthesis, in Silico and in Vitro Dipeptidyl Peptidase‐4 Activity of Triazole‐Based Heterocyclic Compounds
inferred← citeshttps://doi.org/10.1002/cbdv.202503083openalex-snapshot
Unveiling the Potential of Isoquinoline‐Tethered 1,2,3‐Triazoles as Promising Anti‐Biofilm Agents Against Candida albicans : Synthesis, Biological Evaluation, ADME, and Molecular Docking Studies
inferred← citeshttps://doi.org/10.1002/cbic.200500101openalex-snapshot
1,2,3‐Triazole as a Peptide Surrogate in the Rapid Synthesis of HIV‐1 Protease Inhibitors
inferred← citeshttps://doi.org/10.1002/cbic.200800040openalex-snapshot
Peptide Tertiary Structure Nucleation by Side‐Chain Crosslinking with Metal Complexation and Double “Click” Cycloaddition
inferred← citeshttps://doi.org/10.1002/cbic.200800741openalex-snapshot
Enzymatic Glycosylation of Triazole‐Linked GlcNAc/Glc–Peptides: Synthesis, Stability and Anti‐HIV Activity of Triazole‐Linked HIV‐1 gp41 Glycopeptide C34 Analogues
inferred← citeshttps://doi.org/10.1002/cbic.200900198openalex-snapshot
Synthesis and Evaluation of New Thiodigalactoside‐Based Chemical Probes to Label Galectin‐3
inferred← citeshttps://doi.org/10.1002/cbic.200900738openalex-snapshot
Generation of Site‐Specific and Enzymatically Stable Conjugates of Recombinant Proteins with Ubiquitin‐Like Modifiers by the Cu I ‐Catalyzed Azide–Alkyne Cycloaddition
inferred← citeshttps://doi.org/10.1002/cbic.201200200openalex-snapshot
A PEG‐Based Oligomer as a Backbone Replacement for Surface‐Exposed Loops in a Protein Tertiary Structure
inferred← citeshttps://doi.org/10.1002/chem.200701240openalex-snapshot
Multifunctional “Clickates” as Versatile Extended Heteroaromatic Building Blocks: Efficient Synthesis via Click Chemistry, Conformational Preferences, and Metal Coordination
inferred← citeshttps://doi.org/10.1002/chem.200800479openalex-snapshot
“Click Chemistry” in Zeolites: Copper(I) Zeolites as New Heterogeneous and Ligand‐Free Catalysts for the Huisgen [3+2] Cycloaddition
inferred← citeshttps://doi.org/10.1002/chem.200901841openalex-snapshot
A Dual‐Response [2]Rotaxane Based on a 1,2,3‐Triazole Ring as a Novel Recognition Station
inferred← citeshttps://doi.org/10.1002/chem.200902685openalex-snapshot
The Sequential Building of Chiral Macrocyclic Bis‐β‐Lactams by Double Staudinger–Cu‐Catalyzed Azide–Alkyne Cycloadditions
inferred← citeshttps://doi.org/10.1002/chem.201100633openalex-snapshot
Nanometer‐Sized Reactor—A Porphyrin‐Based Model System for Anion Species
inferred← citeshttps://doi.org/10.1002/chem.201102760openalex-snapshot
Amidetriazole: A Versatile Building Block for Construction of Oxyanion Anion Receptors
inferred← citeshttps://doi.org/10.1002/chem.201103393openalex-snapshot
Amine‐Catalyzed [3+2] Huisgen Cycloaddition Strategy for the Efficient Assembly of Highly Substituted 1,2,3‐Triazoles
inferred← citeshttps://doi.org/10.1002/chem.201600928openalex-snapshot
A Practical Guide on the Synthesis of Metal Chelates for Molecular Imaging and Therapy by Means of Click Chemistry
inferred← citeshttps://doi.org/10.1002/chem.201604386openalex-snapshot
Orthogonal Synthesis of Xeno Nucleic Acids
inferred← citeshttps://doi.org/10.1002/chem.201705418openalex-snapshot
Achieving Skeletal Diversity in Peptide Macrocycles through The Use of Heterocyclic Grafts
inferred← citeshttps://doi.org/10.1002/chem.201805919openalex-snapshot
Evaluation of 1,2,3‐Triazoles as Amide Bioisosteres In Cystic Fibrosis Transmembrane Conductance Regulator Modulators VX‐770 and VX‐809
inferred← citeshttps://doi.org/10.1002/chem.201900277openalex-snapshot
Sequential Cu‐Catalyzed Four‐ and Five‐Component Syntheses of Luminescent 3‐Triazolylquinoxalines
inferred← citeshttps://doi.org/10.1002/chem.202000924openalex-snapshot
Single Peptide Backbone Surrogate Mutations to Regulate Angiotensin GPCR Subtype Selectivity
inferred← citeshttps://doi.org/10.1002/chem.202301314openalex-snapshot
Non‐Conjugated Bis‐(Dithienylethene)‐Naphthalenediimide as a Dynamic Anti‐Counterfeiting Agent: Driving the Wheel of Photoswitching Enactment
inferred← citeshttps://doi.org/10.1002/cmdc.201000013openalex-snapshot
Radiofluorinated Pyrimidine‐2,4,6‐triones as Molecular Probes for Noninvasive MMP‐Targeted Imaging
inferred← citeshttps://doi.org/10.1002/cmdc.201100560openalex-snapshot
Fluorogenic Peptide‐Based Substrates for Monitoring Thrombin Activity
inferred← citeshttps://doi.org/10.1002/cmdc.201900622openalex-snapshot
Synthesis, Molecular Docking, and Preliminary Evaluation of 2‐(1,2,3‐Triazoyl)benzaldehydes As Multifunctional Agents for the Treatment of Alzheimer's Disease
inferred← citeshttps://doi.org/10.1002/cmdc.202000220openalex-snapshot
Structural Consequences of the 1,2,3‐Triazole as an Amide Bioisostere in Analogues of the Cystic Fibrosis Drugs VX‐809 and VX‐770
inferred← citeshttps://doi.org/10.1002/cplu.202000791openalex-snapshot
Fluorinated Triazole Foldamers: Folded or Extended Conformational Preferences
inferred← citeshttps://doi.org/10.1002/ejic.201600838openalex-snapshot
Ferrocene–Triazole Combination as a Benchmark for the Electrochemical Detection of Noncovalent Halogen‐Bonding Interactions
inferred← citeshttps://doi.org/10.1002/ejoc.200500216openalex-snapshot
High‐Yielding Microwave‐Assisted Synthesis of Triazole‐Linked Glycodendrimers by Copper‐Catalyzed [3+2] Cycloaddition
inferred← citeshttps://doi.org/10.1002/ejoc.200500483openalex-snapshot
CuI‐Catalyzed Alkyne–Azide “Click” Cycloadditions from a Mechanistic and Synthetic Perspective
inferred← citeshttps://doi.org/10.1002/ejoc.200800143openalex-snapshot
Backbone Amide Linker Strategy for the Synthesis of 1,4‐Triazole‐Containing Cyclic Tetra‐ and Pentapeptides
inferred← citeshttps://doi.org/10.1002/ejoc.200901157openalex-snapshot
CuI‐Catalyzed Azide–Alkyne Intramolecular i‐to‐(i+4) Side‐Chain‐to‐Side‐Chain Cyclization Promotes the Formation of Helix‐Like Secondary Structures
inferred← citeshttps://doi.org/10.1002/ejoc.201100157openalex-snapshot
1,2,3‐Triazoles in Peptidomimetic Chemistry
inferred← citeshttps://doi.org/10.1002/ejoc.201200169openalex-snapshot
Synthesis of a Naphthalene‐diimide Cyclophane for Tuning Supramolecular Interactions by Metal Ions
inferred← citeshttps://doi.org/10.1002/ejoc.201201096openalex-snapshot
Chemoselective Preparation of Unsymmetrical Bis(1,2,3‐triazole) Derivatives and Application in Bis(1,2,3‐triazole)‐Modified Peptidomimetic Synthesis
inferred← citeshttps://doi.org/10.1002/ejoc.201500001openalex-snapshot
A Practical Synthesis of Various 2‐Deoxy‐N‐glycosides by Using D ‐Glucal
inferred← citeshttps://doi.org/10.1002/ejoc.201500360openalex-snapshot
A Facile One‐Pot Metal‐Free Synthesis of 1,4‐Disubstituted 1,2,3‐Triazoles
inferred← citeshttps://doi.org/10.1002/ejoc.201800751openalex-snapshot
A Straightforward Sequential Approach for the Enantioselective Synthesis of Optically Active α‐Arylmethanol‐1,2,3‐Triazoles
inferred← citeshttps://doi.org/10.1002/ejoc.201801320openalex-snapshot
Synthesis, Secondary Structure, and Anion Binding of Acyclic Carbohydrate‐Derived Oligo(amide‐triazole)s
inferred← citeshttps://doi.org/10.1002/ejoc.202200317openalex-snapshot
Regioselective Synthesis of 1,4,5‐Trisubstituted 1,2,3‐Triazole Derivatives from α,β‐Unsaturated Carbonyls
inferred← citeshttps://doi.org/10.1002/hc.21447openalex-snapshot
Synthesis of novel 2‐acetamidothiazoles tethered with 1,2,3‐triazole and pyridine pharmacophores
inferred← citeshttps://doi.org/10.1002/hlca.200890196openalex-snapshot
Synthesis of 1,2,3‐Triazole Analogues of Lincomycin
inferred← citeshttps://doi.org/10.1002/hlca.200900226openalex-snapshot
One‐Pot, Three‐Component Synthesis of 1‐(2‐Hydroxyethyl)‐1H‐1,2,3‐triazole Derivatives by Copper‐Catalyzed 1,3‐Dipolar Cycloaddition of 2‐Azido Alcohols and Terminal Alkynes under Mild Conditions in Water
inferred← citeshttps://doi.org/10.1002/hlca.201100253openalex-snapshot
A One‐Pot Tandem Ugi Multicomponent Reaction (MCR)/Click Reaction as an Efficient Protecting‐Group‐Free Route to 1H‐1,2,3‐Triazole‐Modified α‐Amino Acid Derivatives and Peptidomimetics
inferred← citeshttps://doi.org/10.1002/jbt.21959openalex-snapshot
The evaluation of acute toxicity, antimicrobial activity of 1‐phenyl‐5‐p‐tolyl‐1H‐1, 2, 3‐triazole, and binding to human serum albumin
inferred← citeshttps://doi.org/10.1002/jccs.201190053openalex-snapshot
An Efficient Synthesis of Mono and Bis‐1,2,3‐triazole AZT Derivatives via Copper(I)‐catalyzed Cycloaddition
inferred← citeshttps://doi.org/10.1002/jccs.201700339openalex-snapshot
Cu(OAc)2·H2O/NH2OH·HCl/CH3COONa: A Facile and Efficient Catalyst System for Copper‐catalyzed Azide–Alkyne Click Reactions in Water
inferred← citeshttps://doi.org/10.1002/jhet.1525openalex-snapshot
A Facile One-Pot Route for the General Synthesis of Triazole Linked Chiral 2-Substituted Benzimidazoles
inferred← citeshttps://doi.org/10.1002/jhet.2159openalex-snapshot
Cu(I)‐Catalyzed Efficient Synthesis of 2′‐Triazolo‐nucleoside Conjugates
inferred← citeshttps://doi.org/10.1002/jhet.2365openalex-snapshot
Cu(I)‐Catalyzed Regioselective and Highly Efficient One‐Pot Synthesis of Novel 1,2,3‐Triazoles Decorated with Pyridine and Heterocyclic Amines
inferred← citeshttps://doi.org/10.1002/jhet.2736openalex-snapshot
Design, Synthesis, and Molecular Docking Studies of Pyrazine Containing 1,2,3‐Triazole Derivatives
inferred← citeshttps://doi.org/10.1002/jhet.3426openalex-snapshot
Regioselective N‐Alkylation of Ethyl 4‐Benzyloxy‐1,2,3‐triazolecarboxylate: A Useful Tool for the Synthesis of Carboxylic Acid Bioisosteres
inferred← citeshttps://doi.org/10.1002/jhet.4259openalex-snapshot
Design, synthesis, anticancer activity, and in silico studies of novel imidazo[1,2‐ a ]pyridine based 1 H ‐1,2,3‐triazole derivatives
inferred← citeshttps://doi.org/10.1002/jhet.4545openalex-snapshot
β‐Cyclodextrin‐catalyzed synthesis, characterization, and bacterial evaluation of spirochromanone‐linked 1,2,3‐triazole and spirochromanone conjugates containing bis‐1,2,3‐triazoles
inferred← citeshttps://doi.org/10.1002/jhet.4905openalex-snapshot
Organocatalytic[3 + 2]Cycloaddition: Synthesis of Quinazoline Containing Sulfonyl 1,2,3‐Triazoles as Potent EGFR Targeting Anti‐Breast Cancer Agents
inferred← citeshttps://doi.org/10.1002/mabi.200800220openalex-snapshot
Morphology Controlled Growth of Chitosan‐Bound Microtubes and a Study of their Biocompatibility and Antibacterial Activity
inferred← citeshttps://doi.org/10.1002/macp.200700046openalex-snapshot
Synthesis of Functionalized NMP Initiators for Click Chemistry: A Versatile Method for the Preparation of Functionalized Polymers and Block Copolymers
inferred← citeshttps://doi.org/10.1002/macp.201500209openalex-snapshot
Synthesis, Morphology, and Properties of Polyurethane-triazoles by Click Chemistry
inferred← citeshttps://doi.org/10.1002/marc.200600625openalex-snapshot
‘Click’ Chemistry in Polymer and Materials Science
inferred← citeshttps://doi.org/10.1002/marc.200800089openalex-snapshot
‘Click’ Chemistry in Polymer and Material Science: An Update
inferred← citeshttps://doi.org/10.1002/marc.200800332openalex-snapshot
“Click”‐Chemistry in Polymer and Material Science: the Update
inferred← citeshttps://doi.org/10.1002/marc.201100052openalex-snapshot
Supramolecular Architectures Self‐assembled from Asymmetrical Hetero Cyclopeptides
inferred← citeshttps://doi.org/10.1002/med.20107openalex-snapshot
Click chemistry reactions in medicinal chemistry: Applications of the 1,3‐dipolar cycloaddition between azides and alkynes
inferred← citeshttps://doi.org/10.1002/pola.24563openalex-snapshot
Synthesis of main‐chain poly(carbazole)s via CuAAC
inferred← citeshttps://doi.org/10.1002/psc.1141openalex-snapshot
Side chain‐to‐side chain cyclization by click reaction
inferred← citeshttps://doi.org/10.1002/qsar.200740075openalex-snapshot
Application of the 1,3‐Dipolar Cycloaddition Reaction in Chemical Biology: Approaches Toward Multivalent Carbohydrates and Peptides and Peptide‐Based Polymers
inferred← citeshttps://doi.org/10.1002/qsar.200740112openalex-snapshot
Probing Glycans With the Copper(I)‐Catalyzed [3+2] Azide–Alkyne Cycloaddition
inferred← citeshttps://doi.org/10.1002/slct.201700620openalex-snapshot
Synthesis of 1,2,3‐Triazolo‐fused‐tetrahydro‐β‐carboline Derivatives via 1,3‐Dipolar Cycloaddition Reaction: Cytotoxicity Evaluation and DNA‐Binding studies
inferred← citeshttps://doi.org/10.1002/slct.201800319openalex-snapshot
Click Chemistry Inspired Design, Synthesis and Molecular Docking Studies of Coumarin, Quinolinone Linked 1,2,3‐Triazoles as Promising Anti‐Microbial Agents
inferred← citeshttps://doi.org/10.1002/tcr.202000185openalex-snapshot
Bioactive 1,2,3‐Triazoles: An Account on their Synthesis, Structural Diversity and Biological Applications
inferred← citeshttps://doi.org/10.1007/7081_2014_124openalex-snapshot
Biological Properties of 1H-1,2,3- and 2H-1,2,3-Triazoles
inferred← citeshttps://doi.org/10.1007/7081_2015_192openalex-snapshot
Advances in Merging Triazoles with Peptides and Proteins
inferred← citeshttps://doi.org/10.1007/s00044-009-9215-7openalex-snapshot
A novel approach to the synthesis of 1,2,3-triazoles and their SAR studies
inferred← citeshttps://doi.org/10.1007/s00044-014-1076-zopenalex-snapshot
Synthesis and antibacterial activity of (1-aryl-1, 2, 3-triazol-4-yl) methyl esters of morpholine-3-carboxylic acid
inferred← citeshttps://doi.org/10.1007/s00044-014-1123-9openalex-snapshot
Synthesis and biological evaluation of novel d-glucose-derived 1,2,3-triazoles as potential antibacterial and antifungal agents
inferred← citeshttps://doi.org/10.1007/s00044-015-1361-5openalex-snapshot
Click chemistry inspired synthesis of piperazine-triazole derivatives and evaluation of their antimicrobial activities
inferred← citeshttps://doi.org/10.1007/s00044-017-1789-xopenalex-snapshot
Exploring 1,2,3-triazole derivatives by using in vitro and in silico assays to target new antifungal agents and treat Candidiasis
inferred← citeshttps://doi.org/10.1007/s00044-017-1952-4openalex-snapshot
Synthesis and molecular docking studies of chrysin derivatives as antibacterial agents
inferred← citeshttps://doi.org/10.1007/s00044-017-2072-xopenalex-snapshot
Convenient synthesis, antimalarial and antimicrobial potential of thioethereal 1,4-disubstituted 1,2,3-triazoles with ester functionality
inferred← citeshttps://doi.org/10.1007/s00289-009-0175-3openalex-snapshot
Synthesis and characterization of biocompatible poly(ethylene glycol)-functionalized polyurethane using click chemistry
inferred← citeshttps://doi.org/10.1007/s00706-015-1623-4openalex-snapshot
Metal-free synthesis of 1,2,3-triazoles by azide–aldehyde cycloaddition under ultrasonic irradiation in TSIL [DBU-Bu]OH and in hydrated IL Bu4NOH under heating
inferred← citeshttps://doi.org/10.1007/s00726-011-0941-zopenalex-snapshot
A systematic study of fundamentals in α-helical coiled coil mimicry by alternating sequences of β- and γ-amino acids
inferred← citeshttps://doi.org/10.1007/s00726-013-1663-1openalex-snapshot
Design and synthesis of anti-cancer cyclopeptides containing triazole skeleton
inferred← citeshttps://doi.org/10.1007/s10562-017-2173-7openalex-snapshot
Five-membered N-Heterocycles Synthesis Catalyzed by Nano-silica Supported Copper(II)–2-imino-1,2-diphenylethan-1-ol Complex
inferred← citeshttps://doi.org/10.1007/s10570-022-04637-zopenalex-snapshot
Preparation and properties of azide-modified nitrocellulose and its click reaction curing elastomer
inferred← citeshttps://doi.org/10.1007/s10600-014-0914-zopenalex-snapshot
Azidoisocyanides, New Bifunctional Reagents for Multicomponent Reactions and Biomolecule Modifications
inferred← citeshttps://doi.org/10.1007/s10822-008-9212-9openalex-snapshot
Investigation of structures and properties of cyclic peptide nanotubes by experiment and molecular dynamics
inferred← citeshttps://doi.org/10.1007/s10989-010-9228-6openalex-snapshot
Synthesis of Hybrid Peptidomimetics and Neoglycoconjugates Employing Click Protocol: Dual Utility of Poc-Group for Inserting Carbamate-Triazole Units into Peptide Backbone
inferred← citeshttps://doi.org/10.1007/s11164-015-2241-9openalex-snapshot
Synthesis of new pyrazole-triazole hybrids by click reaction using a green solvent and evaluation of their antitubercular and antibacterial activity
inferred← citeshttps://doi.org/10.1007/s11998-013-9494-2openalex-snapshot
Development of moisture cure polyurethane–urea coatings using 1,2,3-triazole core hyperbranched polyesters
inferred← citeshttps://doi.org/10.1007/s12272-013-0063-0openalex-snapshot
Synthesis and antifungal activity of the novel triazole derivatives containing 1,2,3-triazole fragment
inferred← citeshttps://doi.org/10.1007/s13738-011-0046-3openalex-snapshot
1,4-Dihydroxyanthraquinone-copper(II) nanoparticles immobilized on silica gel: a highly efficient, copper scavenger and recyclable heterogeneous nanocatalyst for a click approach to the three-component synthesis of 1,2,3-triazole derivatives in water
inferred← citeshttps://doi.org/10.1007/s13738-018-1330-2openalex-snapshot
Design, synthesis, activity evaluation and QSAR studies of novel antimalarial 1,2,3-triazolo-β-lactam derivatives
inferred← citeshttps://doi.org/10.1007/s13738-024-03061-3openalex-snapshot
Novel hybrid compounds containing 1,2,3-triazole and naphthalene subunits as xanthine oxidase inhibitors
inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.12565-xopenalex-snapshot
Foldamers in Medicinal Chemistry
inferred← citeshttps://doi.org/10.1016/b978-0-443-18860-2.00021-9openalex-snapshot
Functionalized carbon nanotubes based polymer nanocomposites
inferred← citeshttps://doi.org/10.1016/bs.mie.2016.05.036openalex-snapshot
Designing Covalently Linked Heterodimeric Four-Helix Bundles
inferred← citeshttps://doi.org/10.1016/j.bioorg.2017.01.010openalex-snapshot
Medicinal attributes of 1,2,3-triazoles: Current developments
inferred← citeshttps://doi.org/10.1016/j.bioorg.2017.03.003openalex-snapshot
One-pot synthesis of a new 2-substituted 1,2,3-triazole 1-oxide derivative from dipyridyl ketone and isonitrosoacetophenone hydrazone: Nickel(II) complex, DNA binding and cleavage properties
inferred← citeshttps://doi.org/10.1016/j.bioorg.2018.02.022openalex-snapshot
Potent ACE inhibitors from 5-hydroxy indanone derivatives
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104012openalex-snapshot
β-Turn mimetic synthetic peptides as amyloid-β aggregation inhibitors
inferred← citeshttps://doi.org/10.1016/j.biopha.2010.10.013openalex-snapshot
Thiopurine derivatives containing triazole and steroid: Synthesis, antimalarial and antileishmanial activities
inferred← citeshttps://doi.org/10.1016/j.bmc.2009.12.043openalex-snapshot
Synthesis of 1-(d-glucopyranosyl)-1,2,3-triazoles and their evaluation as glycogen phosphorylase inhibitors
inferred← citeshttps://doi.org/10.1016/j.bmc.2012.01.008openalex-snapshot
A facile ‘click’ approach to novel 15β-triazolyl-5α-androstane derivatives, and an evaluation of their antiproliferative activities in vitro
inferred← citeshttps://doi.org/10.1016/j.bmc.2013.03.063openalex-snapshot
Improving bioorthogonal protein ubiquitylation by click reaction
inferred← citeshttps://doi.org/10.1016/j.bmc.2016.01.027openalex-snapshot
Anionic surfactants enhance click reaction-mediated protein conjugation with ubiquitin
inferred← citeshttps://doi.org/10.1016/j.bmcl.2008.01.102openalex-snapshot
Synthesis and antimicrobial activity of β-lactam–bile acid conjugates linked via triazole
inferred← citeshttps://doi.org/10.1016/j.bmcl.2008.12.026openalex-snapshot
Synthesis and antifungal activity of 1,2,3-triazole containing fluconazole analogues
inferred← citeshttps://doi.org/10.1016/j.bmcl.2011.09.030openalex-snapshot
Synthesis and testing of trifluoromethyl-containing phosphonate–peptide conjugates as inhibitors of serine hydrolases
inferred← citeshttps://doi.org/10.1016/j.bmcl.2013.08.020openalex-snapshot
Systematic replacement of amides by 1,4-disubstituted[1,2,3]triazoles in Leu-enkephalin and the impact on the delta opioid receptor activity
inferred← citeshttps://doi.org/10.1016/j.bmcl.2014.02.027openalex-snapshot
Design and synthesis of novel 2H-chromen-2-one derivatives bearing 1,2,3-triazole moiety as lead antimicrobials
inferred← citeshttps://doi.org/10.1016/j.bmcl.2014.09.036openalex-snapshot
Synthesis and preliminary investigations into novel 1,2,3-triazole-derived androgen receptor antagonists inspired by bicalutamide
inferred← citeshttps://doi.org/10.1016/j.bmcl.2015.08.006openalex-snapshot
Design and synthesis of 11α-substituted bile acid derivatives as potential anti-tuberculosis agents
inferred← citeshttps://doi.org/10.1016/j.bmcl.2017.07.008openalex-snapshot
Synthesis and biological evaluation of novel 1,2,3-triazole derivatives as anti-tubercular agents
inferred← citeshttps://doi.org/10.1016/j.bmcl.2017.08.066openalex-snapshot
Radiosynthesis and biological evaluation of 18F-labeled 4-anilinoquinazoline derivative (18F-FEA-Erlotinib) as a potential EGFR PET agent
inferred← citeshttps://doi.org/10.1016/j.bmcl.2017.10.061openalex-snapshot
Potential antimicrobial agents from triazole-functionalized 2H-benzo[b][1,4]oxazin-3(4H)-ones
inferred← citeshttps://doi.org/10.1016/j.bmcl.2018.02.001openalex-snapshot
Substitution of terminal amide with 1H-1,2,3-triazole: Identification of unexpected class of potent antibacterial agents
inferred← citeshttps://doi.org/10.1016/j.bmcl.2020.127187openalex-snapshot
Radiosynthesis and biological evaluation of an fluorine-18 labeled galactose derivative [18F]FPGal for imaging the hepatic asialoglycoprotein receptor
inferred← citeshttps://doi.org/10.1016/j.bmcl.2021.128331openalex-snapshot
Synthesis and biological evaluation of 1,6-bis-triazole-2,3,4-tri-O-benzyl-α-d-glucopyranosides as a novel α-glucosidase inhibitor in the treatment of Type 2 diabetes
inferred← citeshttps://doi.org/10.1016/j.bmcl.2022.128654openalex-snapshot
Novel indazole skeleton derivatives containing 1,2,3-triazole as potential anti-prostate cancer drugs
inferred← citeshttps://doi.org/10.1016/j.carbpol.2018.07.056openalex-snapshot
Synthesis and antioxidant action of chitosan derivatives with amino-containing groups via azide-alkyne click reaction and N-methylation
inferred← citeshttps://doi.org/10.1016/j.carres.2009.06.039openalex-snapshot
Synthesis of Neu5Ac-Gal-functionalized gold glyconanoparticles
inferred← citeshttps://doi.org/10.1016/j.carres.2010.03.031openalex-snapshot
Synthesis and biological evaluation of glycal-derived novel tetrahydrofuran 1,2,3-triazoles by ‘click’ chemistry
inferred← citeshttps://doi.org/10.1016/j.carres.2010.10.017openalex-snapshot
Application of click chemistry towards an efficient synthesis of 1,2,3-1H-triazolyl glycohybrids as enzyme inhibitors
inferred← citeshttps://doi.org/10.1016/j.carres.2012.01.004openalex-snapshot
Evaluation of bis-triphenylphosphano-copper(I)-butyrate (C3H7COOCu(PPh3)2) as catalyst for the synthesis of 1-glycopyranosyl-4-substituted-1,2,3-triazoles
inferred← citeshttps://doi.org/10.1016/j.carres.2014.10.009openalex-snapshot
Synthesis of 4-amidomethyl-1-glucosyl-1,2,3-triazoles and evaluation as glycogen phosphorylase inhibitors
inferred← citeshttps://doi.org/10.1016/j.carres.2015.07.004openalex-snapshot
An efficient synthesis of novel bis-triazole glycoconjugates via a three-component condensation as a key reaction
inferred← citeshttps://doi.org/10.1016/j.carres.2018.08.015openalex-snapshot
5-Benzoyl triazole as new structural dimension in glycoconjugates
inferred← citeshttps://doi.org/10.1016/j.carres.2019.107751openalex-snapshot
Intramolecular azide-alkene cycloaddition-elimination reaction in an aldohex-2-enonic acid derivative
inferred← citeshttps://doi.org/10.1016/j.cbi.2021.109688openalex-snapshot
1,2,3-Triazole derivatives: synthesis, docking, cytotoxicity analysis and in vivo antimalarial activity
inferred← citeshttps://doi.org/10.1016/j.cclet.2010.11.029openalex-snapshot
Design synthesis and biological evaluation of 3-substituted triazole derivatives
inferred← citeshttps://doi.org/10.1016/j.ccr.2011.06.028openalex-snapshot
The copper(I)-catalyzed alkyne-azide cycloaddition (CuAAC) “click” reaction and its applications. An overview
inferred← citeshttps://doi.org/10.1016/j.comptc.2013.10.008openalex-snapshot
Studies on tautomeric stability and equilibrium of 5(4)-substituted-1,2,3 triazoles. I. Electronegativity and resonance effects of substituent
inferred← citeshttps://doi.org/10.1016/j.ejmech.2013.03.004openalex-snapshot
Optimizing the control of apoptosis by amide/triazole isosteric substitution in a constrained peptoid
inferred← citeshttps://doi.org/10.1016/j.ejmech.2015.12.007openalex-snapshot
Synthesis and biological evaluation of 5,10-dihydro-11 H -dibenzo[ b,e ][1,4]diazepin-11-one structural derivatives as anti-cancer and apoptosis inducing agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2016.08.049openalex-snapshot
Antileishmanial ferrocenylquinoline derivatives: Synthesis and biological evaluation against Leishmania donovani
inferred← citeshttps://doi.org/10.1016/j.ejmech.2017.07.049openalex-snapshot
Click chemistry-based synthesis and anticancer activity evaluation of novel C-14 1,2,3-triazole dehydroabietic acid hybrids
inferred← citeshttps://doi.org/10.1016/j.ejmech.2017.12.012openalex-snapshot
Substrate-derived triazolo- and azapeptides as inhibitors of cathepsins K and S
inferred← citeshttps://doi.org/10.1016/j.ejmech.2018.02.056openalex-snapshot
Molecular interaction of novel benzothiazolyl triazolium analogues with calf thymus DNA and HSA-their biological investigation as potent antimicrobial agents
showing the first 200 of 473 · page through all 473
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.