COMU: scope and limitations of the latest innovation in peptide acyl transfer reagents

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

COMU : scope and limitations of the latest innovation in peptide acyl transfer reagents. / Subirós-Funosas, Ramon; Nieto-Rodriguez, Lidia; Jensen, Knud Jørgen; Albericio, Fernando.

In: Journal of Peptide Science, Vol. 19, No. 7, 2013, p. 408-414.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Subirós-Funosas, R, Nieto-Rodriguez, L, Jensen, KJ & Albericio, F 2013, 'COMU: scope and limitations of the latest innovation in peptide acyl transfer reagents', Journal of Peptide Science, vol. 19, no. 7, pp. 408-414. https://doi.org/10.1002/psc.2517

APA

Subirós-Funosas, R., Nieto-Rodriguez, L., Jensen, K. J., & Albericio, F. (2013). COMU: scope and limitations of the latest innovation in peptide acyl transfer reagents. Journal of Peptide Science, 19(7), 408-414. https://doi.org/10.1002/psc.2517

Vancouver

Subirós-Funosas R, Nieto-Rodriguez L, Jensen KJ, Albericio F. COMU: scope and limitations of the latest innovation in peptide acyl transfer reagents. Journal of Peptide Science. 2013;19(7):408-414. https://doi.org/10.1002/psc.2517

Author

Subirós-Funosas, Ramon ; Nieto-Rodriguez, Lidia ; Jensen, Knud Jørgen ; Albericio, Fernando. / COMU : scope and limitations of the latest innovation in peptide acyl transfer reagents. In: Journal of Peptide Science. 2013 ; Vol. 19, No. 7. pp. 408-414.

Bibtex

@article{c5487518dbbc4461ae7ab80513de8e35,
title = "COMU: scope and limitations of the latest innovation in peptide acyl transfer reagents",
abstract = "The methodology for peptide bond formation is undergoing a continuous evolution where the main actors are being renewed. In recent years, coupling reagents based on the Oxyma scaffold, such as the uronium salt COMU, has been a groundbreaking contribution to the field. The advantages of COMU over classic benzotriazole-based reagents (HATU, HBTU, HCTU, TBTU) were proven in terms of solubility and coupling efficiency in bulky junctions in our groups and others. However, some aspects of the use of COMU need to be revised and improved, such as the stability of commercial samples in organic solvents, which hampers the compatibility with long synthesis in automated synthesizers. In this review, an overview of the main features and suggestions to improve the use of COMU are presented, along with a discussion on the best conditions for its use in microwave-assisted peptide robots.",
author = "Ramon Subir{\'o}s-Funosas and Lidia Nieto-Rodriguez and Jensen, {Knud J{\o}rgen} and Fernando Albericio",
note = "Copyright {\textcopyright} 2013 European Peptide Society and John Wiley & Sons, Ltd.",
year = "2013",
doi = "10.1002/psc.2517",
language = "English",
volume = "19",
pages = "408--414",
journal = "Journal of Peptide Science",
issn = "1075-2617",
publisher = "JohnWiley & Sons Ltd",
number = "7",

}

RIS

TY - JOUR

T1 - COMU

T2 - scope and limitations of the latest innovation in peptide acyl transfer reagents

AU - Subirós-Funosas, Ramon

AU - Nieto-Rodriguez, Lidia

AU - Jensen, Knud Jørgen

AU - Albericio, Fernando

N1 - Copyright © 2013 European Peptide Society and John Wiley & Sons, Ltd.

PY - 2013

Y1 - 2013

N2 - The methodology for peptide bond formation is undergoing a continuous evolution where the main actors are being renewed. In recent years, coupling reagents based on the Oxyma scaffold, such as the uronium salt COMU, has been a groundbreaking contribution to the field. The advantages of COMU over classic benzotriazole-based reagents (HATU, HBTU, HCTU, TBTU) were proven in terms of solubility and coupling efficiency in bulky junctions in our groups and others. However, some aspects of the use of COMU need to be revised and improved, such as the stability of commercial samples in organic solvents, which hampers the compatibility with long synthesis in automated synthesizers. In this review, an overview of the main features and suggestions to improve the use of COMU are presented, along with a discussion on the best conditions for its use in microwave-assisted peptide robots.

AB - The methodology for peptide bond formation is undergoing a continuous evolution where the main actors are being renewed. In recent years, coupling reagents based on the Oxyma scaffold, such as the uronium salt COMU, has been a groundbreaking contribution to the field. The advantages of COMU over classic benzotriazole-based reagents (HATU, HBTU, HCTU, TBTU) were proven in terms of solubility and coupling efficiency in bulky junctions in our groups and others. However, some aspects of the use of COMU need to be revised and improved, such as the stability of commercial samples in organic solvents, which hampers the compatibility with long synthesis in automated synthesizers. In this review, an overview of the main features and suggestions to improve the use of COMU are presented, along with a discussion on the best conditions for its use in microwave-assisted peptide robots.

U2 - 10.1002/psc.2517

DO - 10.1002/psc.2517

M3 - Journal article

C2 - 23712932

VL - 19

SP - 408

EP - 414

JO - Journal of Peptide Science

JF - Journal of Peptide Science

SN - 1075-2617

IS - 7

ER -

ID: 99345129