An efficient, convenient solid-phase synthesis of amino acid-modified peptide nucleic acid monomers and oligomers

Bioconjugate Chemistry

Volumn 17, Issue 2, 2006, Pages 551-558

  Balaji, Baghavathy S ^a   Gallazzi, Fabio ^a   Jia, Fang ^a   Lewis, Michael R ^a,b,c,d  

^a UNIVERSITY OF MISSOURI   (United States)

^b University of Missouri   (United States)

^c VETERANS AFFAIRS MEDICAL CENTER   (United States)

^d UNIVERSITY OF MISSOURI   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACIDS; CHLORINE COMPOUNDS; NUCLEIC ACIDS; OLIGOMERS; PEPTIDES; PURIFICATION; SYNTHESIS (CHEMICAL);

ACIDIC AMINO ACIDS; AMINO-ACIDS; BASIC AMINO ACIDS; HIGHER YIELD; HYDROPHILICS; PEPTIDE NUCLEIC ACID; SOLID PHASE SYNTHESIS; SOLID PHASIS; SOLID-PHASE; VERSATILE METHODS;

MONOMERS;

ACETALDEHYDE; AMINO ACID; CHLORIDE; ESTER; ETHER DERIVATIVE; FUNCTIONAL GROUP; MESSENGER RNA; MONOMER; NUCLEIC ACID BASE; OLIGOMER; PEPTIDE NUCLEIC ACID; PURINE; PYRIMIDINE; RESIN; WATER;

ALKYLATION; ARTICLE; ELECTROSPRAY MASS SPECTROMETRY; HYBRIDIZATION; PROTON NUCLEAR MAGNETIC RESONANCE; REVERSED PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; SOLID PHASE SYNTHESIS; SOLUBILITY;

EID: 33645468612     PISSN: 10431802     EISSN: None     Source Type: Journal    
DOI: 10.1021/bc0502208     Document Type: Article

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