Zobrazeno 1 - 10
of 1 546
pro vyhledávání: '"J.-L. Imbach"'
Publikováno v:
In Antiviral Research 2000 46(1):A62-A62
Publikováno v:
In Antiviral Research 2000 46(1):A62-A62
Publikováno v:
In Antiviral Research 2000 46(1):A62-A62
Publikováno v:
In Antiviral Research 2000 46(1):A62-A62
Publikováno v:
In Antiviral Research 2000 46(1):A56-A56
Publikováno v:
In Antiviral Research 2000 46(1):A55-A55
Publikováno v:
In Antiviral Research 2000 46(1):A35-A35
Publikováno v:
Molecules, Vol 5, Iss 10, Pp 1139-1145 (2000)
The E- and Z- phosphonoalkenyl acyclonucleosides of uracil and thymine were synthesized under Michael addition conditions. Introduction of an alkyl, alkenyl or alkynyl group at the N-3 position of the pyrimidine moiety was accomplished using potassiu
Externí odkaz:
https://doaj.org/article/694eee5d484f403bb95cfcd81bb8627e
Publikováno v:
Antiviral Chemistry and Chemotherapy. 12:223-232
We report the synthesis, in vitro anti-HIV-1 activity and stability study of a mononucleoside phosphotriester derivative of 3′-azido-2′,3′-dideoxythymidine (AZT) bearing a new biolabile phosphate-protection, namely S-pivaloyl-2-thioisopropyl (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c4acded30702adf41c81f9d6ecbcaa2
https://doi.org/10.1177/095632020101200403
https://doi.org/10.1177/095632020101200403
Publikováno v:
Molecules, Vol 5, Iss 10, Pp 1139-1145 (2000)
Molecules
Volume 5
Issue 10
Pages 1139-1145
Molecules
Volume 5
Issue 10
Pages 1139-1145
The E- and Z- phosphonoalkenyl acyclonucleosides of uracil and thymine were synthesized under Michael addition conditions. Introduction of an alkyl, alkenyl or alkynyl group at the N-3 position of the pyrimidine moiety was accomplished using potassiu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28f9a195dd143a98eb13a7e1bcb535fa
http://www.mdpi.com/1420-3049/5/10/1139/
http://www.mdpi.com/1420-3049/5/10/1139/