The oxime bond formation as an efficient chemical tool for the preparation of 3′,5′-bifunctionalised oligodeoxyribonucleotides

Bioorganic and Medicinal Chemistry Letters

Volumn 14, Issue 11, 2004, Pages 2839-2842

  Edupuganti, Om Prakash ^a   Renaudet, Olivier ^a   Defrancq, Eric ^a   Dumy, Pascal ^a  

^a UNIVERSITÉ JOSEPH FOURIER   (France)

Author keywords

Chemoselectivity; Conjugation; Oligonucleotide; Oxime

Indexed keywords

ALDEHYDE; CARBOHYDRATE; DISACCHARIDE; MONOSACCHARIDE; OLIGODEOXYNUCLEOTIDE DERIVATIVE; OXIME DERIVATIVE; PEPTIDE;

ACIDITY; ARTICLE; CHEMICAL BOND; CONJUGATION; DRUG STRUCTURE; DRUG SYNTHESIS; PROTECTION; STEREOCHEMISTRY;

CARBOHYDRATES; CROSS-LINKING REAGENTS; HUMANS; LACTOSE; MANNOSE; NUCLEAR LOCALIZATION SIGNALS; OLIGODEOXYRIBONUCLEOTIDES; OLIGOPEPTIDES; OXIMES; PEPTIDES; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 2342452008     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2004.03.053     Document Type: Article

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