Synthesis of a cyclopentane amide DNA analogue and its base pairing properties


Autoria(s): Ahn, D. R.; Mosimann, Markus; Leumann, Christian
Data(s)

2003

Resumo

cpa-DNA monomers containing the bases adenine and thymine have been synthesized starting from the known compound 1 in 12 steps. Partially and fully modified cpa-thymidine and cpa-adenosine containing oligodeoxynucleotides were synthesized by standard oligonucleotide chemistry. Fully modified homo-cpa-A sequences lead to duplex destabilization by -1.4 degrees C/mod. relative to DNA. As its congener bca-DNA, cpa-DNA prefers left-handed duplex formation where possible

Formato

application/pdf

Identificador

http://boris.unibe.ch/68575/1/10833737.pdf

Ahn, D. R.; Mosimann, Markus; Leumann, Christian (2003). Synthesis of a cyclopentane amide DNA analogue and its base pairing properties. Nucleosides, nucleotides & nucleic acids, 22(5-8), pp. 1207-1210. Taylor & Francis 10.1081/NCN-120022837 <http://dx.doi.org/10.1081/NCN-120022837>

doi:10.7892/boris.68575

info:doi:10.1081/NCN-120022837

urn:issn:1525-7770

Idioma(s)

eng

Publicador

Taylor & Francis

Relação

http://boris.unibe.ch/68575/

Direitos

info:eu-repo/semantics/restrictedAccess

Fonte

Ahn, D. R.; Mosimann, Markus; Leumann, Christian (2003). Synthesis of a cyclopentane amide DNA analogue and its base pairing properties. Nucleosides, nucleotides & nucleic acids, 22(5-8), pp. 1207-1210. Taylor & Francis 10.1081/NCN-120022837 <http://dx.doi.org/10.1081/NCN-120022837>

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

info:eu-repo/semantics/article

info:eu-repo/semantics/publishedVersion

PeerReviewed