Advanced search
1 file | 4.04 MB Add to list

Recent trends in Cys- and Ser/Thr-based synthetic strategies for the elaboration of peptide constructs

(2012) CHEMICAL COMMUNICATIONS. 48(95). p.11601-11622
Author
Organization
Abstract
Recent conceptual advances in the chemical synthesis of peptide constructs are described, encompassing native chemical ligation (i.e. the chemoselective covalent condensation of unprotected peptide segments) and O-, S-acyl isopeptide strategies (i.e. internal O,S-to-N acyl transfer within peptides).
Keywords
O-ACYL ISOPEPTIDE, NATIVE CHEMICAL LIGATION, PRIOR THIOL CAPTURE, SEQUENCE-CONTAINING PEPTIDES, INTRAMOLECULAR O, N-ACYL TRANSFER, AMIDE BOND FORMATION, KINETICALLY CONTROLLED LIGATION, EXPRESSED PROTEIN LIGATION, BIOLOGY-ORIENTED SYNTHESIS, ISLET AMYLOID POLYPEPTIDE

Downloads

  • (...).pdf
    • full text
    • |
    • UGent only
    • |
    • PDF
    • |
    • 4.04 MB

Citation

Please use this url to cite or link to this publication:

MLA
Monbaliu, Jean-Christophe, and Alan Katritzky. “Recent Trends in Cys- and Ser/Thr-based Synthetic Strategies for the Elaboration of Peptide Constructs.” CHEMICAL COMMUNICATIONS 48.95 (2012): 11601–11622. Print.
APA
Monbaliu, J.-C., & Katritzky, A. (2012). Recent trends in Cys- and Ser/Thr-based synthetic strategies for the elaboration of peptide constructs. CHEMICAL COMMUNICATIONS, 48(95), 11601–11622.
Chicago author-date
Monbaliu, Jean-Christophe, and Alan Katritzky. 2012. “Recent Trends in Cys- and Ser/Thr-based Synthetic Strategies for the Elaboration of Peptide Constructs.” Chemical Communications 48 (95): 11601–11622.
Chicago author-date (all authors)
Monbaliu, Jean-Christophe, and Alan Katritzky. 2012. “Recent Trends in Cys- and Ser/Thr-based Synthetic Strategies for the Elaboration of Peptide Constructs.” Chemical Communications 48 (95): 11601–11622.
Vancouver
1.
Monbaliu J-C, Katritzky A. Recent trends in Cys- and Ser/Thr-based synthetic strategies for the elaboration of peptide constructs. CHEMICAL COMMUNICATIONS. 2012;48(95):11601–22.
IEEE
[1]
J.-C. Monbaliu and A. Katritzky, “Recent trends in Cys- and Ser/Thr-based synthetic strategies for the elaboration of peptide constructs,” CHEMICAL COMMUNICATIONS, vol. 48, no. 95, pp. 11601–11622, 2012.
@article{3100761,
  abstract     = {Recent conceptual advances in the chemical synthesis of peptide constructs are described, encompassing native chemical ligation (i.e. the chemoselective covalent condensation of unprotected peptide segments) and O-, S-acyl isopeptide strategies (i.e. internal O,S-to-N acyl transfer within peptides).},
  author       = {Monbaliu, Jean-Christophe and Katritzky, Alan},
  issn         = {1359-7345},
  journal      = {CHEMICAL COMMUNICATIONS},
  keywords     = {O-ACYL ISOPEPTIDE,NATIVE CHEMICAL LIGATION,PRIOR THIOL CAPTURE,SEQUENCE-CONTAINING PEPTIDES,INTRAMOLECULAR O,N-ACYL TRANSFER,AMIDE BOND FORMATION,KINETICALLY CONTROLLED LIGATION,EXPRESSED PROTEIN LIGATION,BIOLOGY-ORIENTED SYNTHESIS,ISLET AMYLOID POLYPEPTIDE},
  language     = {eng},
  number       = {95},
  pages        = {11601--11622},
  title        = {Recent trends in Cys- and Ser/Thr-based synthetic strategies for the elaboration of peptide constructs},
  url          = {http://dx.doi.org/10.1039/c2cc34434c},
  volume       = {48},
  year         = {2012},
}

Altmetric
View in Altmetric
Web of Science
Times cited: