A short, efficient synthesis of 2'-deoxypseudoisocytidine based on Heck-chemistry


Autoria(s): Mayer, Alain; Leumann, Christian
Data(s)

2003

Resumo

A novel synthesis of 2'-deoxypseudoisocytidine as well as of its phosphoramidite building block for oligonucleotide synthesis is presented. The synthesis is based on Heck-coupling between N-protected pseudoisocytosine and a silyl protected furanoid glycal. With this procedure the corresponding phosphoramidite building block is obtained in 5 steps and an overall yield of 28%.

Formato

application/pdf

Identificador

http://boris.unibe.ch/68563/1/NCN-120025239.pdf

Mayer, Alain; Leumann, Christian (2003). A short, efficient synthesis of 2'-deoxypseudoisocytidine based on Heck-chemistry. Nucleosides, nucleotides & nucleic acids, 22(10), pp. 1919-1925. Taylor & Francis 10.1081/NCN-120025239 <http://dx.doi.org/10.1081/NCN-120025239>

doi:10.7892/boris.68563

info:doi:10.1081/NCN-120025239

info:pmid:14609231

urn:issn:1525-7770

Idioma(s)

eng

Publicador

Taylor & Francis

Relação

http://boris.unibe.ch/68563/

Direitos

info:eu-repo/semantics/restrictedAccess

Fonte

Mayer, Alain; Leumann, Christian (2003). A short, efficient synthesis of 2'-deoxypseudoisocytidine based on Heck-chemistry. Nucleosides, nucleotides & nucleic acids, 22(10), pp. 1919-1925. Taylor & Francis 10.1081/NCN-120025239 <http://dx.doi.org/10.1081/NCN-120025239>

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

info:eu-repo/semantics/article

info:eu-repo/semantics/publishedVersion

PeerReviewed