Synthetic studies towards a novel, chemical stable, abasic site analogue of DNA


Autoria(s): Hirtz, C.; Leumann, Christian
Data(s)

2003

Resumo

We synthesized the phosphinate 7 via photoaddition of methanol to the alpha, beta unsaturated deoxyribono lactone as the key step, followed by an Arbusov reaction for the introduction of phosphorous. Precursor 7 serves for the synthesis and incorporation into DNA of a novel chemically stable abasic site analogue that might act as an inhibitor for DNA glycosylases

Formato

application/pdf

Identificador

http://boris.unibe.ch/68565/1/10833738.pdf

Hirtz, C.; Leumann, Christian (2003). Synthetic studies towards a novel, chemical stable, abasic site analogue of DNA. Nucleosides, nucleotides & nucleic acids, 22(5-8), pp. 1203-1206. Taylor & Francis 10.1081/NCN-120022836 <http://dx.doi.org/10.1081/NCN-120022836>

doi:10.7892/boris.68565

info:doi:10.1081/NCN-120022836

info:pmid:14565380

urn:issn:1525-7770

Idioma(s)

eng

Publicador

Taylor & Francis

Relação

http://boris.unibe.ch/68565/

Direitos

info:eu-repo/semantics/restrictedAccess

Fonte

Hirtz, C.; Leumann, Christian (2003). Synthetic studies towards a novel, chemical stable, abasic site analogue of DNA. Nucleosides, nucleotides & nucleic acids, 22(5-8), pp. 1203-1206. Taylor & Francis 10.1081/NCN-120022836 <http://dx.doi.org/10.1081/NCN-120022836>

Palavras-Chave #570 Life sciences; biology #540 Chemistry
Tipo

info:eu-repo/semantics/article

info:eu-repo/semantics/publishedVersion

PeerReviewed