Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Okamura, Noriaki"'
Autor:
小嶋, 智, Kojima, Satoru, 岡村, 祝明, Okamura, Noriaki, 大谷, 具幸, Ohtani, Tomoyuki, 鈴木, 和博, Suzuki, Kazuhiro, 野崎, 保, Nozaki, Tamotsu, 永田, 秀尚, Nagata, Hidehisa
第20回名古屋大学年代測定総合研究センターシンポジウム平成19(2007)年度報告 Proceedings of the 20th symposiumon on Chronological Studies at the Nagoya University Center for Chronological Research in 2007 日時:平成20 (2
Externí odkaz:
http://hdl.handle.net/2237/13732
^<14>C age of buried stump preserved in dammed lake sediments of Koinami in Yatsuo Town, Toyama City, central Japan(Proceedings of the 20^ Symposium on Chronological Studies at the Nagoya University Center for Chronological Research in 2007)
Autor:
Kojima, Satoru, Okamura, Noriaki, Ohtani, Tomoyuki, Suzuki, Kazuhiro, Nozaki, Tamotsu, Nagata, Hidehisa
Publikováno v:
名古屋大学加速器質量分析計業績報告書. 19:90-98
Koinami in Yatsuo Town, Toyama City, central Japan is located on a small flat basin along the Besso River surrounded by ridges about 600-800 m in altitude, south of the Toyama Plain. The ENE-WSW trending fault to the south of Koinami is the boundary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=jairo_______::ddee01d3e770d6ccd4bbede958a7126e
https://nagoya.repo.nii.ac.jp/records/11859
https://nagoya.repo.nii.ac.jp/records/11859
Autor:
Okamura Noriaki, K. Tomimori, Kenji Manabe, Kiyoshi Bannai, Y. Kato, A. Hazato, S. Sugiura, Toshio Tanaka, Seizi Kurozumi, Ryoji Noyori
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f6e5b0094613670b66f2f4168f9707c
https://doi.org/10.1002/chin.199101351
https://doi.org/10.1002/chin.199101351
Autor:
Satoshi Sugiura, Toshio Tanaka, Okamura Noriaki, Yoshinori Kato, Kenji Manabe, Koji Tomimori, Kiyoshi Bannai, Ryoji Noyori, Seizi Kurozumi, Atsuo Hazato
Publikováno v:
Tetrahedron. 46:6689-6704
Syntheses of isocarbacyclin (20) using highly regioselective alkylation of the new allylic alcohol intermediate 6 having an exocyclic double bond are described. The allylic alcohol 6 was prepared by (i) allylic rearrangement of the allylic alcohol 3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e3479169429a3c3133f4faf2f597698
https://doi.org/10.1016/s0040-4020(01)87859-5
https://doi.org/10.1016/s0040-4020(01)87859-5
Akademický článek
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Autor:
Tanaka, Toshio, Oba, Takeo, Okamura, Noriaki, Watanabe, Kenzo, Kurozumi, Seizi, Naruchi, Tatsuyuki
Publikováno v:
Synthetic Communications; Jan1980, Vol. 10 Issue 10, p773-789, 17p
Autor:
Atsuo Hazato, Kiyoshi Bannai, Toshio Kawagishi, Satoshi Sugiura, Kenji Manabe, Ryoji Noyori, Takeshi Toru, Okamura Noriaki, Masaaki Suzuki, Toshio Tanaka, Seizi Kurozumi
Publikováno v:
Tetrahedron. 43:813-824
The nitro-olefin trapping of the enolates in situ generated by conjugate addition of organocopper reagents to the chiral oxygenated cyclopentenone synthon, R-4, gives the three-component coupling products in a regiospecific manner. The intermediary n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e31fe91ae430570ffe6a899e9a719eb
https://doi.org/10.1016/s0040-4020(01)90018-3
https://doi.org/10.1016/s0040-4020(01)90018-3
Autor:
Kiyoshi Bannai, Takeo Ba, Seizi Kurozumi, Okamura Noriaki, Takeshi Toru, Toshio Tanaka, Kenzo Watanabe
Publikováno v:
Tetrahedron Letters. 22:1417-1420
Stable analogues of PGI2, 7-hydroxy- and 7-acetoxy-PGI2, were synthesized from protected PGI2 methyl ester 1b via sulfoxides 6a , 6b through stereocontrolled sulfoxide-sulfenate rearrangement.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::caead763291b687b57bbceb000741996
https://doi.org/10.1016/s0040-4039(01)90337-5
https://doi.org/10.1016/s0040-4039(01)90337-5
Autor:
Takeo Ōba, Atsuo Hazato, Okamura Noriaki, Seizi Kurozumi, Takeshi Toru, Kenzo Watanabe, Toshio Tanaka, Kiyoshi Bannai
Publikováno v:
Tetrahedron. 39:3807-3819
Syntheses of several stable PGI2 analogs substituted by an electron-withdrawing substituent at C-5 or C-7 are described. Reaction of PGI2 methyl ester ( 1 ) with benzenesulfenyl chloride gave (5E)-5-phenylthio-PGI2 ( 2 ) or (5 R)-5-phenylthio-Δ6-PGI
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a4c4730daa4baef88560ed1d84053b0
https://doi.org/10.1016/s0040-4020(01)88623-3
https://doi.org/10.1016/s0040-4020(01)88623-3