Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Naoko Hirose"'
Autor:
Hirotaka SHIOZAKI, Satoshi YOKOSE, Masaki SAITOU, Yoh SUZUKI, Naoko HIROSE, Hideyuki SHIMIZU, Kenji MASUDA, Akihiko HASEGAWA, Tadashi KATAYAMA, Yasuhiko OKUMURA
Publikováno v:
Journal of Japanese Society for Laser Dentistry. 16:23-30
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0ffffbe1c584eefa93314e862e91ff0
https://doi.org/10.5984/jjpnsoclaserdent.16.23
https://doi.org/10.5984/jjpnsoclaserdent.16.23
Autor:
Naoko Hirose, Satoshi Katayama, Satoshi Takamatsu, Marc Demillequand, Geert Schelkens, Kunisuke Izawa, Jozef Brepoels, Etienne De Cock
Publikováno v:
Nucleosides, Nucleotides and Nucleic Acids. 21:849-861
Perfluoroalkanesulfonyl fluorides are effective dehydroxy-fluorination agents for the hydroxyl group at the sugar moiety of nucleoside derivatives and give the corresponding fluorinated nucleosides in good yield with an inversion of configuration in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6ce273a796a33451ff1b54c4aed9f85
https://doi.org/10.1081/ncn-120016572
https://doi.org/10.1081/ncn-120016572
Publikováno v:
Tetrahedron Letters. 42:7605-7608
Hypophosphorous acid and dialkyl phosphites are effective radical reducing agents for O-thiocarbonyl groups or halides at the sugar part of nucleoside derivatives and give the corresponding hydrocarbons in high yield.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4f5325a093357c2b8510d0f7bbbfeb4d
https://doi.org/10.1016/s0040-4039(01)01617-3
https://doi.org/10.1016/s0040-4039(01)01617-3
Autor:
Kunisuke Izawa, Naoko Hirose, Masakazu Nakazawa, Takayoshi Torii, Yasuyuki Otake, Tomoyuki Onishi, Takashi Nakano
Publikováno v:
Tetrahedron Letters. 42:6337-6340
Dihalomethylation of several N-protected amino acid esters gave N-protected α-aminoalkyl-α′-dihalomethylketones, which are useful intermediates for the synthesis of erythro β-amino-α-hydroxycarboxylic acids, in good yield. The dihalomethylketon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a8eb87358251fd5da4ef42d138658aa4
https://doi.org/10.1016/s0040-4039(01)01253-9
https://doi.org/10.1016/s0040-4039(01)01253-9
Publikováno v:
Tetrahedron Letters. 42:5887-5890
Chloromethylation of N -imine-protected amino acid esters followed by acid hydrolysis gave α-aminoalkyl-α′-chloromethylketone as a HCl salt form in good yield without racemization. The amino group was conveniently protected with carbamate protect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f616d30df9b0cc6a72a635da55af90c
https://doi.org/10.1016/s0040-4039(01)01115-7
https://doi.org/10.1016/s0040-4039(01)01115-7
Autor:
Satoshi Takamatsu, Tokumi Maruyama, Satoshi Katayama, Naoko Hirose, Masaki Naito, Kunisuke Izawa
Publikováno v:
Tetrahedron Letters. 42:2325-2328
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::278e5500b9eb5adc859cc685207526e6
https://doi.org/10.1016/s0040-4039(01)00136-8
https://doi.org/10.1016/s0040-4039(01)00136-8
Publikováno v:
Tetrahedron Letters. 42:2321-2324
An improved synthesis of 9-(2,3-dideoxy-2-fluoro-β- d - threo -pentofuranosyl)adenine ( 1 , FddA) via a fluorination of 3′- O -benzoyl-5′- O -tritylriboside ( 4a ) using noncorrosive triethylamine trihydrofluoride (Et 3 N·3HF) is described. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d5cd2560556e6e7f196e3aac35671732
https://doi.org/10.1016/s0040-4039(01)00135-6
https://doi.org/10.1016/s0040-4039(01)00135-6
Publikováno v:
ChemInform. 32
An improved synthesis of 9-(2,3-dideoxy-2-fluoro-β- d - threo -pentofuranosyl)adenine ( 1 , FddA) via a fluorination of 3′- O -benzoyl-5′- O -tritylriboside ( 4a ) using noncorrosive triethylamine trihydrofluoride (Et 3 N·3HF) is described. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ccff3ddf9b67fa01287d312795c74fd3
https://doi.org/10.1002/chin.200127204
https://doi.org/10.1002/chin.200127204
Autor:
Tokumi Maruyama, Satoshi Katayama, Kunisuke Izawa, Naoko Hirose, Masaki Naito, Satoshi Takamatsu
Publikováno v:
ChemInform. 32
A synthesis of 9-(2,3-dideoxy-2-fluoro-beta-D-threo-pentofuranosyl)adenine (1, FddA) via a 6-chloro-9-(3-deoxy-beta-D-erythro-pentofuranosyl)-9H-purine (9), which was readily obtained from inosine (5), is described. Fluorination at the C2'-beta posit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4fe66b602fa6d3da587a7198d9984bf1
https://doi.org/10.1002/chin.200127205
https://doi.org/10.1002/chin.200127205
Publikováno v:
ChemInform. 32
Chloromethylation of N -imine-protected amino acid esters followed by acid hydrolysis gave α-aminoalkyl-α′-chloromethylketone as a HCl salt form in good yield without racemization. The amino group was conveniently protected with carbamate protect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cbbba6ff232ead9a8f477032c0152cd7
https://doi.org/10.1002/chin.200149164
https://doi.org/10.1002/chin.200149164