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NEW TRENDS IN PEPTIDE COUPLING REAGENTS

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Ynamide‐Mediated Peptide Bond Formation: Mechanistic Study and Synthetic Applications

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A new polymer-supported reagent for the Fmoc-protection of amino acids

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Amino acid chlorides: a journey from instability and racemization toward broader utility in organic synthesis including peptides and their mimetics

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Synthesis of peptides mediated by KOBt

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Synthesis of medium-ring lactams and macrocyclic peptide mimetics via conjugate addition/ring expansion cascade reactions

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New Strategies for an Efficient Removal of the 9-Fluorenylmethoxycarbonyl (Fmoc) Protecting Group in the Peptide Synthesis

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Improved solid‐phase synthesis of α,α‐dialkylated amino acid‐rich peptides with antimicrobial activity*

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N-Silylation of amines and amino acid esters under neutral conditions employing TMS-Cl in the presence of zinc dust

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N-Urethane protection of amines and amino acids in an ionic liquid

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A model reaction for assessing the coupling and chiral efficiency of reagents in depside bond formation

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Palladium-catalyzed synthesis of amides and peptides

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Synthesis of Fmoc-amino acid chlorides assisted by ultrasonication, a rapid approach

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Rapid and efficient synthesis of peptide fragments containing α-aminoisobutyric acid using Fmoc-amino acid chlorides/potassium salt of 1-hydroxybenzotriazole

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Screening of N‐Alkyl‐Cyanoacetamido Oximes as Substitutes for N‐Hydroxysuccinimide

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Synthesis of Fmoc-amino acid chlorides assisted by ultrasonication, a rapid approach

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Preparation of 2‐alkoxy‐4‐alkyl‐5(4H)‐oxazolones from mixed anhydrides of N‐alkoxycarbonylamino acids

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Configuration and racemization determination of cysteine residues in peptides by chiral derivatization and HPLC: application to oxytocin peptides

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Synthesis and NMR Analysis of a Conformationally Controlled β-Turn Mimetic Torsion Balance

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(9H‐Fluoren‐9‐yl)methanesulfonyl (Fms): An Amino Protecting Group Complementary to Fmoc

Ishibashi, Y., Miyata, K., & Kitamura, M. (2010) · European Journal of Organic Chemistry · doi:10.1002/ejoc.201000682 · Cited by 10 · see citing works

Facile synthesis of colorimetric histone deacetylase substrates

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1.6 Peptides and Chirality Effects on the Conformation and the Synthesis of Medicinally Relevant Peptides

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1-(t-Butyldimethylsilyloxy) benzotriazole (TBDMS-OBt): A new and novel reagent for the synthesis of peptides

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1-(t-butyldimethylsilyloxy) benzotriazole (TBDMS-OBt): A new and novel reagent for the synthesis of peptides

Tantry, S. J., & Babu, V. V. S. (2002) · International Journal of Peptide Research and Therapeutics · doi:10.1007/bf02538305 · Cited by 7 · see citing works

ChemInform Abstract: ((9‐Fluorenylmethyl)oxy)carbonyl Amino Acid Chlorides in Solid‐Phase Peptide Synthesis.

Carpino, L. A., CAHO, H. G., Beyermann, M., & Bienert, M. (1991) · ChemInform · doi:10.1002/chin.199139225 · Cited by 6 · see citing works

N‐9‐Fluorenylmethoxycarbonylpyroglutamate

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Peptide Synthesis with α-(Difluoromethyl)-Substituted α-Amino Acids

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Avoiding the Hidden Costs of Peptide Synthesis: THIQ in DMI as an Alternative Fmoc-Deprotection Reagent

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A Promising Compound for Green Multiresponsive Materials Based on Acyl Carrier Protein

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Ynamide‐Mediated Peptide Bond Formation: Mechanistic Study and Synthetic Applications

Xu, S., Jiang, D., Peng, Z., Hu, L., Liu, T., Zhao, L., & Zhao, J. (2022) · Angewandte Chemie · doi:10.1002/ange.202212247 · Cited by 4 · see citing works

Peptide bond formation via an intramolecular rearrangement

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Rapid and efficient synthesis of peptides containing α,α-dialkylamino acids employing KOBt

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Fmoc-Peptide Acid Chlorides in Fragment Coupling: Synthesis of β-Casomorphin by 3+2 Divergent Approach

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1-Hydroxybenzotriazole

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12 Pushing the Limits of Solid-Phase Peptide Synthesis with Continuous Flow

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Synthesis of Cholic Acid-Peptide Conjugates With A Negatively Charged Ester Linkage for Oral Delivery

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HOBt·DCHA-Mediated Synthesis of Sterically Hindered Peptides employing Fmoc-Amino Acid Chlorides in Both Solution-Phase and Solid Phase Methods

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Chemical Synthesis of Peptides and Polypeptides

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Premature removal of Nα-9-fluorenylmethyloxycarbonyl in thermodynamically controlled enzymatic coupling trials

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Rapid and Efficient Synthesis of Peptides Containing α,α-dialkylamino acids employing KOBt

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TwoN-ortho-nitrobenzenesulfonyl α,α-disubstituted amino acid adducts

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Synthesis of Peptides Employing Protected-Amino Acid Halides Mediated by Commercial Anion Exchange Resin

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K. M. Sivanandaiah: Twenty-Five Years of Peptide Research in Central College, Bangalore University, Bangalore, India

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Design and synthesis of novel antisense nucleopeptides and their biophysical evaluation

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Use of N-Fmoc amino acid chlorides and 2-alkoxy-5(4H)- oxazolones in solid phase peptide synthesis

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Peptide Synthesis

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1-Hydroxybenzotriazole

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Single-Cell Recognition and Separation via Matched Reciprocating-Flow Interfaces and Peptide Recognition Dynamics

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ChemInform Abstract: ((9‐Fluorenylmethyl)oxy)carbonyl Amino Acid Chlorides in Solid‐Phase Peptide Synthesis.

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Fmoc-amino acid chlorides-KOBt in solid phase peptide synthesis

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(Fluoren-9-ylmethoxy)carbonyl (Fmoc) amino acid chlorides. Synthesis, characterization, and application to the rapid synthesis of short peptide segments

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In situ generation of Fmoc amino acid chlorides for extremely difficult couplings to sterically hindered secondary amines in solid-phase peptide synthesis

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ChemInform Abstract: Fmoc‐Amino Acid Chlorides in Solid Phase Synthesis of Opioid Peptides.

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