Oxyma: An Efficient Additive for Peptide Synthesis to Replace the Benzotriazole‐Based HOBt and HOAt with a Lower Risk of Explosion[1]
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- 14 September 2009
- journal article
- research article
- Published by Wiley in Chemistry – A European Journal
- Vol. 15 (37), 9394-9403
- https://doi.org/10.1002/chem.200900614
Abstract
Oxyma [ethyl 2-cyano-2-(hydroxyimino)acetate] has been tested as an additive for use in the carbodiimide approach for formation of peptide bonds. Its performance in relation to those of HOBt and HOAt, which have recently been reported to exhibit explosive properties, is reported. Oxyma displayed a remarkable capacity to inhibit racemization, together with impressive coupling efficiency in both automated and manual synthesis, superior to those of HOBt and at least comparable to those of HOAt, and surpassing the latter coupling agent in the more demanding peptide models. Stability assays showed that there was no risk of capping the resin under standard coupling conditions. Finally, calorimetry assays (DSC and ARC) showed decomposition profiles for benzotriazole-based additives that were consistent with their reported explosivities and suggested a lower risk of explosion in the case of Oxyma.Keywords
This publication has 26 references indexed in Scilit:
- Morpholine-Based Immonium and Halogenoamidinium Salts as Coupling Reagents in Peptide Synthesis1The Journal of Organic Chemistry, 2008
- Novel Proton Acceptor Immonium-Type Coupling Reagents: Application in Solution and Solid-Phase Peptide SynthesisOrganic Letters, 2007
- Explosive properties of 1-hydroxybenzotriazolesJournal of Hazardous Materials, 2005
- Bis(tetramethylene)fluoroformamidinium Hexafluorophosphate(BTFFH): A Convenient Coupling Reagent for Solid Phase Peptide SynthesisChemistry Letters, 1998
- Glycopeptide Synthesis UsingO-Pentafluorophenyluronium Salts as novel condensing reagentsAdvanced Synthesis & Catalysis, 1998
- Recent Developments in the Assessment of Thermal Risks of Chemical ProcessesOrganic Process Research & Development, 1997
- Carbodiimide-Mediated Amide Formation in a Two-Phase System. A High-Yield and Low-Racemization Procedure for Peptide SynthesisThe Journal of Organic Chemistry, 1995
- Tetramethylfluoroformamidinium Hexafluorophosphate: A Rapid-Acting Peptide Coupling Reagent for Solution and Solid Phase Peptide SynthesisJournal of the American Chemical Society, 1995
- A basic strategy for the thermal stability assessment of pharmaceutical synthetic intermediates and productsJournal of Thermal Analysis and Calorimetry, 1991
- Peptides. IV. Racemization Suppression by the Use of Ethyl 2-Hydroximino-2-cyanoacetate and Its AmideBulletin of the Chemical Society of Japan, 1973