Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Youji Furukawa"'
Publikováno v:
Bioorganic & Medicinal Chemistry. 12:3561-3567
Enantiomerically pure (R)- and (S)-1-(1H-1,2,4-triazol-1-yl)-2-(4-fluorophenyl)-3-trimethylsilylpropan-2-ol 1 were prepared via an enantioselective Grignard reaction. The absolute stereochemistry of 1 was determined by X-ray analysis. In a comparison
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d0dbcf9c6d9e9ce1dfaae282f9c78c6
https://doi.org/10.1016/j.bmc.2004.04.027
https://doi.org/10.1016/j.bmc.2004.04.027
Autor:
Youji Furukawa, Masahiro Ikeda, Yasuo Shimoji, Yoshiko Kitahara, Shuichi Miyamoto, Yoshiya Amemiya, Takuro Kanazaki, Toshio Sada, Makoto Mizuno, Hiroyuki Koike, Fujimoto Koichi, Hiroaki Yanagisawa
Publikováno v:
Journal of Medicinal Chemistry. 39:323-338
A series of imidazole-5-carboxylic acids bearing alkyl, alkenyl, and hydroxyalkyl substituents at the 4-position and their related compounds were prepared and evaluated for their antagonistic activities to the angiotensin II (AII) receptor. Among the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd4cd3308fb04385c4957345c80d3f42
https://doi.org/10.1021/jm950450f
https://doi.org/10.1021/jm950450f
Autor:
Atsushi Kasuya, Masami Arai, Masao Shiozaki, Shuichi Miyamoto, Hideyuki Haruyama, Youji Furukawa, Tomoko Takayama, Yoshiyuki Kobayashi
Publikováno v:
The Journal of Organic Chemistry. 59:4450-4460
6-epi-Trehazolin was synthetized in a stereocontrolled manner, and this synthesis proved that an oxazine structural isomer of 6-epi-trehazolin does not exist
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9cc00b2335e3324eae2524c0080836f
https://doi.org/10.1021/jo00095a021
https://doi.org/10.1021/jo00095a021
Autor:
Shigeki Muramatsu, Youji Furukawa, Satoru Naito, Yasuo Nakada, Junya Ide, Tadashi Hata, Akio Saito
Publikováno v:
The Journal of Antibiotics. 47:812-820
Epoxidation reactions (MCPBA epoxidation and Sharpless epoxidation) were examined as a means of chemically modifying milbemycins as part of our program for discovering anthelmintics. 8, 9-Epoxy-, 14, 15-epoxy-, 8, 9-14, 15-diepoxy-, and 3, 4-8, 9-14,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d60781335bc6b867e35ff7a72db89d5d
https://doi.org/10.7164/antibiotics.47.812
https://doi.org/10.7164/antibiotics.47.812
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::104073c9ad8c6ff312f22a7195c6bf20
https://doi.org/10.1002/chin.199126255
https://doi.org/10.1002/chin.199126255
Autor:
Atsushi Kasuya, Tomoko Takayama, Shuichi Miyamoto, Yoshiyuki Kobayashi, Masao Shiozaki, Masami Arai, Youji Furukawa, Hideyuki Haruyama
Publikováno v:
ChemInform. 26
6-epi-Trehazolin was synthetized in a stereocontrolled manner, and this synthesis proved that an oxazine structural isomer of 6-epi-trehazolin does not exist
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16deece892da4a987a4d60de0f8efd04
https://doi.org/10.1002/chin.199506229
https://doi.org/10.1002/chin.199506229
Autor:
Yasuo Nakada, Shigeki Muramatsu, Junya Ide, Akio Saito, Satoru Naito, Tadashi Hata, Youji Furukawa
Publikováno v:
ChemInform. 26
Epoxidation reactions (MCPBA epoxidation and Sharpless epoxidation) were examined as a means of chemically modifying milbemycins as part of our program for discovering anthelmintics. 8, 9-Epoxy-, 14, 15-epoxy-, 8, 9-14, 15-diepoxy-, and 3, 4-8, 9-14,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bbd2c2494a1bc2611ebf9f7c8f8952f9
https://doi.org/10.1002/chin.199505290
https://doi.org/10.1002/chin.199505290
Autor:
Natsuki Tanaka, Takeshi Kagasaki, Tadashi Hata, Shuji Takahashi, Akio Torikata, Fujimoto Katsumi, Youji Furukawa, Shiozawa Hideyuki
Publikováno v:
ChemInform. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ede9acc7fb20bcf600616ad6580570a
https://doi.org/10.1002/chin.199604279
https://doi.org/10.1002/chin.199604279
Autor:
Takeshi Kinoshita, Youji Furukawa, Masatoshi Inukai, Mizuka Nakayama, Hiroshi Kogen, Toshihiro Kiho
Publikováno v:
ChemInform. 32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e42fbf3856495ae519caa37759b0e3ed
https://doi.org/10.1002/chin.200107171
https://doi.org/10.1002/chin.200107171
Publikováno v:
ChemInform. 41
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f14c97cdb7b447403566d88896c4a45
https://doi.org/10.1002/chin.201009200
https://doi.org/10.1002/chin.201009200