At the dated check, the references listed below either did not resolve in
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The 107 checked references that resolve
resolves10.1021/cr040669eProteases Universally Recognize Beta Strands In Their Active Sites
resolves10.1038/154703a0Gramicidin S and its use in the Treatment of Infected Wounds
resolves10.1038/nrd2590The exploration of macrocycles for drug discovery — an underexploited structural class
resolves10.1002/bip.21372Invited reviewnative chemical ligation applied to the synthesis and bioengineering of circular peptides and proteins
resolves10.1021/cr0301402Macrolactonizations in the Total Synthesis of Natural Products
resolves10.1021/ja00497a032Chemistry of polymer-bound o-benzyne. Frequency of encounter between substituents on crosslinked polystyrenes
resolves10.1002/psc.512On‐resin head‐to‐tail cyclization of cyclotetrapeptides: optimization of crucial parameters
resolves10.1002/anie.200461656Head‐to‐Tail Peptide Cyclodimerization by Copper‐Catalyzed Azide–Alkyne Cycloaddition
resolves10.1021/cr950005sChemical Synthesis of Natural Product Peptides: Coupling Methods for the Incorporation of Noncoded Amino Acids into Peptides
resolves10.1021/ja00049a021Prediction of the best linear precursor in the synthesis of cyclotetrapeptides by molecular mechanic calculations
resolves10.1002/anie.196503561Synthesis of Cyclotri‐<scp>L</scp>‐prolyl, a Cyclotripeptide Having a Nine‐Membered Ring
resolves10.1021/ja984016pStructural Mimicry of Canonical Conformations in Antibody Hypervariable Loops Using Cyclic Peptides Containing a Heterochiral Diproline Template
resolves10.1021/ja00076a005Biomimetic synthesis of gramicidin S. Direct formation of the antibiotic from pentapeptide active esters having no protecting group on the side chain of the Orn residue
resolves10.1021/jo01332a003Practical synthesis of cyclic peptides, with an example of dependence of cyclization yield upon linear sequence
resolves10.1021/jo951108dCyclization of<i>all</i>-<scp>l</scp>-Pentapeptides by Means of 1-Hydroxy-7-azabenzotriazole-Derived Uronium and Phosphonium Reagents
resolves10.1021/ja970855kConformational Analysis of Reverse-Turn Constraints by N-Methylation and N-Hydroxylation of Amide Bonds in Peptides and Non-Peptide Mimetics
resolves10.1021/ja063123d<i>N</i>-Methylated Cyclic Pentaalanine Peptides as Template Structures
resolves10.1002/chem.200701029Conformational Preference and Potential Templates of <i>N</i>‐Methylated Cyclic Pentaalanine Peptides
resolves10.1021/ja017160aKinetic Control of Proline Amide Rotamers: Total Synthesis of <i>trans,trans</i>- and <i>cis,cis</i>-Ceratospongamide
resolves10.1021/ja961509qPseudo-Prolines as a Solubilizing, Structure-Disrupting Protection Technique in Peptide Synthesis
resolves10.1021/ja962780aPseudo-Prolines as a Molecular Hinge: Reversible Induction of<i>cis</i>Amide Bonds into Peptide Backbones
resolves10.1021/jo0484732Pseudoprolines as Removable Turn Inducers: Tools for the Cyclization of Small Peptides
resolves10.1021/ol101018wSynthesis of All-<scp>l</scp>Cyclic Tetrapeptides Using Pseudoprolines as Removable Turn Inducers
resolves10.1021/jo052027cCarbosilane Dendrimeric Carbodiimides: Site Isolation as a Lactamization Tool
resolves10.1039/b813439aMolecularly imprinted cavities template the macrocyclization of tetrapeptides
resolves10.1021/mp700137gNonribosomal Peptide Synthetases Involved in the Production of Medically Relevant Natural Products
resolves10.1021/cb700233tReprogramming the Translation Initiation for the Synthesis of Physiologically Stable Cyclic Peptides
resolves10.1002/hlca.19890720502Solubilization of Peptides in Non‐polar Organic Solvents by the Addition of Inorganic Salts: Facts and Implications
resolves10.1034/j.1399-3011.2000.00734.xSelective and facile cyclization of <i>N</i>‐chloroacetylated peptides from the C4 domain of HIV Gp120 in LiCl/DMF solvent systems
resolves10.1073/pnas.78.7.4055New segment-coupling method for peptide synthesis in aqueous solution: application to synthesis of human [Gly17]-beta-endorphin.
resolves10.1021/ja983859dLactone and Lactam Library Synthesis by Silver Ion-Assisted Orthogonal Cyclization of Unprotected Peptides
resolves10.1021/cc900100zSynthesis of Cyclic Peptides through Direct Aminolysis of Peptide Thioesters Catalyzed by Imidazole in Aqueous Organic Solutions
resolves10.1021/ol100596pMacrolactonization of Peptide Thioesters Catalyzed by Imidazole and Its Application in the Synthesis of Kahalalide B and Analogues
resolves10.1039/c001375gOn-resin peptide macrocyclization using thiol–ene click chemistry
resolves10.1021/ja954278gCyclic Peptides from Linear Unprotected Peptide Precursors through Thiazolidine Formation
resolves10.1021/ja9621105Synthesis and Application of Unprotected Cyclic Peptides as Building Blocks for Peptide Dendrimers
resolves10.1039/a702083jChemoselective backbone cyclization of unprotected peptides
resolves10.1021/jo049839dOn-Resin Native Chemical Ligation for Cyclic Peptide Synthesis<sup>1</sup><sup>,</sup><sup>2</sup>
resolves10.1002/1521-3773(20011001)40:19<3625::AID-ANIE3625>3.0.CO;2-QDesign and Synthesis of a Protein Catenane This work was supported by The Skaggs Institute for Chemical Biology, The Sloan Foundation, and NIH-GM570132 (PED). We thank Dr. Songpong Deechongkit for assistance with the analytical ultracentrifuge and CD measurements.
resolves10.1021/ja984480uThia Zip Reaction for Synthesis of Large Cyclic Peptides: Mechanisms and Applications
resolves10.1021/ja003265mSynthesis of Peptides and Proteins without Cysteine Residues by Native Chemical Ligation Combined with Desulfurization
resolves10.1021/ja992173ySynthesis of Difficult Cyclic Peptides by Inclusion of a Novel Photolabile Auxiliary in a Ring Contraction Strategy
resolves10.1039/b800464aCyclic tetrapeptides via the ring contraction strategy: chemical techniques useful for their identification
resolves10.1021/ol034907oDifficult Macrocyclizations: New Strategies for Synthesizing Highly Strained Cyclic Tetrapeptides
resolves10.1021/ja962260fConformational Control by Thiazole and Oxazoline Rings in Cyclic Octapeptides of Marine Origin. Novel Macrocyclic Chair and Boat Conformations
resolves10.1021/jo011148jPeptidotriazoles on Solid Phase: [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides
resolves10.1021/ol053095oClick Chemistry as a Route to Cyclic Tetrapeptide Analogues: Synthesis of<i>c</i><i>yclo</i>-[Pro-Val-ψ(triazole)-Pro-Tyr]
resolves10.1039/b616751a1,2,3-Triazoles as peptide bond isosteres: synthesis and biological evaluation of cyclotetrapeptide mimics
resolves10.1021/ol702228uClick Chemistry as a Macrocyclization Tool in the Solid-Phase Synthesis of Small Cyclic Peptides
resolves10.1021/ol0518028Efficient Route to<i>C</i><sub>2</sub>Symmetric Heterocyclic Backbone Modified Cyclic Peptides
resolves10.1002/anie.200805901Conformationally Homogeneous Heterocyclic Pseudotetrapeptides as Three‐Dimensional Scaffolds for Rational Drug Design: Receptor‐Selective Somatostatin Analogues
resolves10.1021/ja075865sProtein Prosthesis: 1,5-Disubstituted[1,2,3]triazoles as <i>cis</i>-Peptide Bond Surrogates
resolves10.1021/ja054114sRuthenium-Catalyzed Cycloaddition of Alkynes and Organic Azides
resolves10.1002/anie.200805900Probing the Bioactive Conformation of an Archetypal Natural Product HDAC Inhibitor with Conformationally Homogeneous Triazole‐Modified Cyclic Tetrapeptides
resolves10.1002/anie.200904980Cyclative Cleavage through Dipolar Cycloaddition: Polymer‐Bound Azidopeptidylphosphoranes Deliver Locked <i>cis‐</i>Triazolylcyclopeptides as Privileged Protein Binders
resolves10.1021/ja961626lApplication of Ring-Closing Metathesis to the Synthesis of Rigidified Amino Acids and Peptides
resolves10.1021/ja000563aAn All-Hydrocarbon Cross-Linking System for Enhancing the Helicity and Metabolic Stability of Peptides
resolves10.1021/ja0466659A Highly Stable Short α-Helix Constrained by a Main-Chain Hydrogen-Bond Surrogate
resolves10.1021/ja062710wEvaluation of Biologically Relevant Short α-Helices Stabilized by a Main-Chain Hydrogen-Bond Surrogate
resolves10.1021/ol702521gDesign and Synthesis of Cyclic RGD Pentapeptoids by Consecutive Ugi Reactions
resolves10.1039/b210952bVia Ugi reactions to conformationally fixed cyclic peptidesDedicated to Professor Dr D. Seebach on the occasion of his 65th birthday.
resolves10.1021/ja100517vTotal Synthesis of Cyclosporine: Access to N-Methylated Peptides via Isonitrile Coupling Reactions
resolves10.1021/ja028485+Highly Stable Self-Assembly in Water: Ion Pair Driven Dimerization of a Guanidiniocarbonyl Pyrrole Carboxylate Zwitterion
resolves10.1021/ja910544pMacrocyclization of Linear Peptides Enabled by Amphoteric Molecules
resolves10.1021/ja805649fTranslation of DNA into a Library of 13 000 Synthetic Small-Molecule Macrocycles Suitable for <i>in Vitro</i> Selection
resolves10.1021/ja063722kHigh-Throughput Sequence Determination of Cyclic Peptide Library Members by Partial Edman Degradation/Mass Spectrometry
resolves10.1039/b415578ePhotolithographic synthesis of cyclic peptide arrays using a differential deprotection strategy
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