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Synthesis and In Vitro Characterization of Glycopeptide Drug Candidates Related to PACAP1–23

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Dipropylamine for 9-Fluorenylmethyloxycarbonyl (Fmoc) Deprotection with Reduced Aspartimide Formation in Solid-Phase Peptide Synthesis

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Carpino's protecting groups, beyond the Boc and the Fmoc

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Improved preparation of amyloid‐β peptides using DBU as Nα‐Fmoc deprotection reagent

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The Degradation of Corticotropin-releasing Factor by Enzymes of the Rat Brain Studied by Liquid Chromatography–Mass Spectrometry

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Dramatically enhanced N→O acyl migration during the trifluoroacetic acid-based deprotection step in solid phase peptide synthesis

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Convergent Solid‐Phase Synthesis of N‐Glycopeptides Facilitated by Pseudoprolines at Consensus‐Sequence Ser/Thr Residues

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The effect of dibenzofuran substitutions in corticotropin-releasing factor

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p‐Nitrobenzyloxycarbonyl (pNZ) as a Temporary Nα‐Protecting Group in Orthogonal Solid‐Phase Peptide Synthesis – Avoiding Diketopiperazine and Aspartimide Formation

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Fmoc-Removal with Pyrrolidine Expands the Available Solvent Space in Green Solid-Phase Peptide Synthesis

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Solid-Phase Synthesis of C-Terminus Cysteine Peptide Acids

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Influence of α-helicity, amphipathicity and D-amino acid incorporation on the peptide-induced mast cell activation

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Comparative studies of Nsc and Fmoc asNα-protecting groups for SPPS

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Synthesis of truncated analogues of preptin-(1–16), and investigation of their ability to stimulate osteoblast proliferation

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Structure‐activity relationship studies of shortened analogues of the antimicrobial peptide EeCentrocin 1 from the sea urchin Echinus esculentus

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On the use of N‐dicyclopropylmethyl aspartyl‐glycine synthone for backbone amide protection

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Convergent Solid‐Phase Synthesis of N‐Glycopeptides Facilitated by Pseudoprolines at Consensus‐Sequence Ser/Thr Residues

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New t‐butyl based aspartate protecting groups preventing aspartimide formation in Fmoc SPPS

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Unexpected aspartimude formation during coupling reactions using Asp(OAl) in solid-phase peptide synthesis

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Characterization of the Ca2+-coordination structures of L- and T-plastins in combination with their synthetic peptide analogs by FTIR spectroscopy

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Corticotropin-releasing hormone (CRH) receptors in the mesenteric small arteries of rats resemble the (2)-subtype

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Biochemical Pharmacology, 1996, 52, 829
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Characterization of a multi-lipopeptides mixture used as an HIV-1 vaccine candidate

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Solid-phase synthesis of tailed cyclic peptides: The use of α-allyl-protected aspartic acid leads to aspartimide and tetramethylguanidinium formation

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Sequence dependence of aspartimide formation during 9-fluorenylmethoxycarbonyl solid-phase peptide synthesis

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Microwave-assisted solid-phase peptide synthesis of neurosecretory protein GL composed of 80 amino acid residues

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Solid-phase peptide synthesis: from standard procedures to the synthesis of difficult sequences

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EDOTn and MIM, new peptide backbone protecting groups

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Design of protecting groups for the β‐carboxylic group of aspartic acid that minimize base‐catalyzed aspartimide formation

AMELIE KARLSTRÖM and ANDERS UNDÉN

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Expediting the Fmoc solid phase synthesis of long peptides through the application of dimethyloxazolidine dipeptides

Peter White, John W. Keyte, Kevin Bailey and Graham Bloomberg

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Synthesis of cyclic herpes simplex virus peptides containing 281-284 epitope of glycoprotein D-1 inendo- orexo-position

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Design and Synthesis of Brain Penetrant Glycopeptide Analogues of PACAP With Neuroprotective Potential for Traumatic Brain Injury and Parkinsonism

Christopher R. Apostol, Kelsey Bernard, Parthasaradhireddy Tanguturi, Gabriella Molnar, Mitchell J. Bartlett, Lajos Szabò, Chenxi Liu, J. Bryce Ortiz, Maha Saber, Katherine R. Giordano, Tabitha R. F. Green, James Melvin, Helena W. Morrison, Lalitha Madhavan, Rachel K. Rowe, John M. Streicher, Michael L. Heien, Torsten Falk and Robin Polt

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Structure–activity relationship of marinostatin, a serine protease inhibitor isolated from a marine organism

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α- and β- aspartyl peptide ester formationvia aspartimide ring opening

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N‐Butylpyrrolidinone for Solid‐Phase Peptide Synthesis is Environmentally Friendlier and Synthetically Better than DMF

Ashish Kumar, Mahama Alhassan, John Lopez, Fernando Albericio and Beatriz G. de la Torre

ChemSusChem, 2020, 13, 5288
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Thirteen decades of peptide synthesis: key developments in solid phase peptide synthesis and amide bond formation utilized in peptide ligation

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13C‐markierte Tyrosinreste als lokale IR‐Sonden zur Analyse konformativer Änderungen in Peptiden und Proteinen

Sandra Tremmel, Michael Beyermann, Hartmut Oschkinat, Michael Bienert, Dieter Naumann and Heinz Fabian

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Solid‐phase synthesis and on‐resin cyclization of a disulfide bond peptide and lactam analogues corresponding to the major antigenic site of HIV gp41 protein

D. Limal, J.‐P Briand, P. Dalbon and M. Jolivet

The Journal of Peptide Research, 1998, 52, 121
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Acid-Mediated Prevention of Aspartimide Formation in Solid Phase Peptide Synthesis

Tillmann Michels, Rudolf Dölling, Uwe Haberkorn and Walter Mier

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3-(1-Piperidinyl)alanine formation during the preparation ofC-terminal cysteine peptides with the Fmoc/t-Bu strategy

Jan Lukszo, Dale Patterson, Fernando Albericio and Steven A. Kates

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Rearrangement of Glu(OtBu)- and Asp(OtBu)-containing peptides upon fluoride treatment in solid-phase synthesis

Steven A. Kates and Fernando Albericio

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Higher-order Molecular Packing in Amyloid-like Fibrils Constructed with Linear Arrangements of Hydrophobic and Hydrogen-bonding Side-chains

Masatoshi Saiki, Shinya Honda, Kazunori Kawasaki, Deshan Zhou, Akira Kaito, Takeo Konakahara and Hisayuki Morii

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Advances in Fmoc solid‐phase peptide synthesis

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Solid‐Supported Synthesis of Highly Functionalized Tripodal Peptides with Flexible but Preorganized Geometry: Towards Potential Serine Protease Mimics

An Gea, Nadia Farcy, Núria Roqué i Rossell, José C. Martins, Pierre J. De Clercq and Annemieke Madder

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A new strategy for the synthesis of Asp-Gly units-containing glycopeptides using Fmoc/Bzl protection

Hong Mang, Yali Wang and Wolfgang Voelter

Tetrahedron Letters, 1995, 36, 8767
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Synthesis of complex head-to-side-chain cyclodepsipeptides

Marta Pelay-Gimeno, Fernando Albericio and Judit Tulla-Puche

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Analysis of the conserved glycosylation site in the nicotinic acetylcholine receptor: potential roles in complex assembly

Keith W. Rickert and Barbara Imperiali

Chemistry & Biology, 1995, 2, 751
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Synthesis and applications of a new base-labile fluorene derived linker for solid-phase peptide synthesis

Francesc Rabanal, Ernest Giralt and Fernando Albericio

Tetrahedron, 1995, 51, 1449
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Synthesis of peptide sequences related to thrombospondin: factors affecting aspartimide by‐product formation

J. Cebrián, V. Domingo and F. Reig

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Comparative Endocrinology, 2016, 42, 65
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Amino Acid-Protecting Groups

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Chem. Rev., 2009, 109, 2455
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Investigation on side-product formation during the synthesis of a lactoferrin-derived lactam-bridged cyclic peptide

Maria Carmina Scala, Antonia Spensiero, Giacomo Pepe, Alessia Bertamino, Alfonso Carotenuto, Paolo Grieco, Ettore Novellino, Isabel M. Gomez-Monterrey, Pietro Campiglia and Marina Sala

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