Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Kunisuke Kawasaki-shi Izawa"'
Autor:
Jerzy Boryski, Johan Neyts, Tomoyuki Onishi, Joanna Fogt, Erik De Clercq, Kunisuke Kawasaki-shi Izawa, Piotr Januszczyk
Publikováno v:
Nucleosides, Nucleotides & Nucleic Acids. 28:713-723
A series of novel 2'-C-methylribonucleosides, involving 5-iodo and 5-alkynyl uridine analogues as well as related bicyclic furano- and pyrrolo[2,3-d]pyrimidinone compounds, has been synthesized and evaluated for their inhibitory effect on replication
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::329efbfc8211608a1edadcbacbe974ef
https://doi.org/10.1080/15257770903128870
https://doi.org/10.1080/15257770903128870
Autor:
Tokumi Maruyama, Yoshiko Satoh, Kunisuke Kawasaki-shi Izawa, Satoshi Takamatsu, Shigetada Kozai
Publikováno v:
Chemical and Pharmaceutical Bulletin. 47:966-970
A facile and practicam method to infroduce fluorine at the up-side of the 2'-carbon of nucleosides is described. 6-Chloropurine riboside 3 was converted to the 3'-O-benzoate 4a via a stannylene complex, then converted to the 3'-O-benzoyl-5'-O-tritylr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e4066efa64cf1dc7ba203411144dee3
https://doi.org/10.1248/cpb.47.966
https://doi.org/10.1248/cpb.47.966
Autor:
Tokumi Maruyama, Kunisuke Kawasaki-shi Izawa, Yoshiko Satoh, Shigetada Kozai, Satoshi Takamatsu
Publikováno v:
ChemInform. 30
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f7a37cfb0c9f0149919203faef6db5e8
https://doi.org/10.1002/chin.199948228
https://doi.org/10.1002/chin.199948228
Autor:
Piotr Januszczyk, Jerzy Boryski, Johan Neyts, Tomoyuki Onishi, Kunisuke Kawasaki-shi Izawa, Joanna Fogt, Erik De Clercq
Publikováno v:
ChemInform. 41
A series of novel 2′-C-methylribonucleosides, involving 5-iodo and 5-alkynyl uridine analogues as well as related bicyclic furano- and pyrrolo[2,3-d]pyrimidinone compounds, has been synthesized and evaluated for their inhibitory effect on replicati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::53881637d757b6ef15b949ea50236f34
https://doi.org/10.1002/chin.201002217
https://doi.org/10.1002/chin.201002217
Publikováno v:
Organic letters. 4(24)
[reaction: see text] A practical method for the synthesis of optically active styrene oxides has been developed via formation of optically active 2-chloro-1-phenylethanols generated by reductive transformation of ring-substituted 2-chloroacetophenone
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7aa466e89bec957d08ac65fe95a5f3d
https://pubmed.ncbi.nlm.nih.gov/12443101
https://pubmed.ncbi.nlm.nih.gov/12443101