Margaret Brimble
brimble.chem.auckland.ac.nz
0000-0002-7086-4096
University of Auckland
561 papers found
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Cover Feature: A Versatile Boc Solid Phase Synthesis of Daptomycin and Analogues Using Site Specific, On‐Resin Ozonolysis to Install the Kynurenine Residue (Chem. Eur. J. 62/2019)
A Versatile Boc Solid Phase Synthesis of Daptomycin and Analogues Using Site Specific, On‐Resin Ozonolysis to Install the Kynurenine Residue
Synthesis of the Tetracyclic Cores of the Integrastatins, Epicoccolide A and Epicocconigrone A
Synthesis and Evaluation of Novel TLR2 Agonists as Potential Adjuvants for Cancer Vaccines
Organic Synthesis: Where to from Now? A Personal Perspective from Down Under
Pharmacological Characterization and Investigation of N-Terminal Loop Amino Acids of Adrenomedullin 2 That Are Important for Receptor Activation
Naturally Occurring Lumazines
Highly Diastereoselective Synthesis of Syn ‐1,3‐Dihydroxyketone Motifs from Propargylic Alcohols via Spiroepoxide Intermediates
Glucoregulatory activity of vesiculin in insulin sensitive and resistant mice
Site-specific glycation of Aβ1–42 affects fibril formation and is neurotoxic
Very Short and Stable Lactoferricin-Derived Antimicrobial Peptides: Design Principles and Potential Uses
Investigations of the key macrolactamisation step in the synthesis of cyclic tetrapeptide pseudoxylallemycin A
Convenient access to 5-membered cyclic iminium ions: evidence for a stepwise [4 + 2] cycloaddition mechanism
A chiral auxiliary-based synthesis of the C5–C17 trans-decalin framework of anthracimycin
Synthesis of endolides A and B: naturally occurring N-methylated cyclic tetrapeptides
A synthetic approach to ‘click’ neoglycoprotein analogues of EPO employing one-pot native chemical ligation and CuAAC chemistry
Benzannulated spiroketal natural products: isolation, biological activity, biosynthesis, and total synthesis
Efficient synthesis and characterisation of the amyloid beta peptide, Aβ1–42, using a double linker system
Enhancing T cell responses and tumour immunity by vaccination with peptides conjugated to a weak NKT cell agonist
Frontispiece: Chemical Synthesis of Bioactive Naturally Derived Cyclic Peptides Containing Ene‐Like Rigidifying Motifs
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