Enhancing solid phase synthesis by a noncovalent protection strategy-efficient coupling of rhodamine to resin-bound peptide nucleic acids

Citation
Ld. Mayfield et Dr. Corey, Enhancing solid phase synthesis by a noncovalent protection strategy-efficient coupling of rhodamine to resin-bound peptide nucleic acids, BIOORG MED, 9(10), 1999, pp. 1419-1422
Citations number
5
Categorie Soggetti
Chemistry & Analysis
Journal title
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
ISSN journal
0960894X → ACNP
Volume
9
Issue
10
Year of publication
1999
Pages
1419 - 1422
Database
ISI
SICI code
0960-894X(19990517)9:10<1419:ESPSBA>2.0.ZU;2-4
Abstract
Resins for solid-phase synthesis can affect coupling efficiencies by intera cting with reactants. We have observed that polyethylene glycol-polystyrene (PEG-PS) solid support absorbs added activated fluorophores, preventing ef ficient labeling of peptide nucleic acids (PNAs). We now report that additi on of an inexpensive unactivated fluorophore blocks the resin and allows ef ficient labeling. This protection strategy may have general benefits for pe ptide and combinatorial synthesis, (C) 1999 Elsevier Science Ltd. All right s reserved.