Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Norihiro Ikemoto"'
Autor:
Yuri Natori, Yoshiaki Kinase, Norihiro Ikemoto, Fabio Spaziani, Tsutomu Kojima, Hitomi Kakuta, Junko Fujita, Kazuyuki Someya, Katsuyoshi Tatenuma, Toshiyo Yabuta, Hiroki Takakuwa, Koichi Otsuki
Publikováno v:
C, Vol 7, Iss 4, p 86 (2021)
An iodine-doped activated carbon (named IodAC) was developed by adsorbing molecular iodine (I2) on commercially available activated carbon (AC). Iodine was selected with the purpose to add its well-known antibacterial and antiviral properties to the
Externí odkaz:
https://doaj.org/article/c328d50f60fd4dd79626ed117559f410
Autor:
Shunya Nakasone, Masahiro Tanaka, Yuji Ishizu, Norihiro Ikemoto, Masahide Furukawa, Yoshitaka Shiroma, Naofumi Akata
Publikováno v:
Japanese Journal of Health Physics. 53:65-71
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::378a1e1a4cf732263ba1aaaff524f873
https://doi.org/10.5453/jhps.53.65
https://doi.org/10.5453/jhps.53.65
Autor:
Yuri Natori, Katsuyoshi Tatenuma, Kazuo Yonehara, Masanori Hara, Tomohiko Kawakami, Norihiro Ikemoto
Publikováno v:
Fusion Engineering and Design. 158:111701
Molecular sieves (MSs) are a potentially useful means of hydrogen isotope recovery as well as the temporary storage and supply of such isotopes. In this study, the hydrogen adsorption isotherms for various MS samples were acquired after applying diff
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3cbe84cfb9029729a4b948d2cd5204bb
https://doi.org/10.1016/j.fusengdes.2020.111701
https://doi.org/10.1016/j.fusengdes.2020.111701
Autor:
Andrew W. Gibson, Fouzia Machrouhi, Doug E. Frantz, Michael H. Kress, Cameron J. Cowden, Norihiro Ikemoto, Todd D. Nelson, Anthony Alorati, Brian C. Bishop, Karsten Menzel, Matthew S. Bodenstein
Publikováno v:
Organic Process Research & Development. 13:519-524
As part of Merck’s continued research effort on inflammation and pain, a safe synthesis of an orally bioavailable and CNS penetrant bradykinin 1 antagonist was developed and demonstrated on kilogram scale. The key step included a novel regioselecti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5eb0bb70c0e7ab820b36abed78023be
https://doi.org/10.1021/op8003184
https://doi.org/10.1021/op8003184
Autor:
Norihiro Ikemoto, Ross A. Miller, Jinchu Liu, Benjamin Marcune, Joseph Laquidara, Ralph P. Volante, Joseph D. Armstrong, Petrillo Daniel E, Fred J. Fleitz, Joseph F. Leone, Sandor Karady
Publikováno v:
Tetrahedron Letters. 46:1867-1871
Two syntheses of the title compound 1 were developed based on different approaches for installing the oxazole ring moiety. Formation and dehydration of ketoamide was initially used and scaled up to afford 1 on several kilogram scale, then oxazolyl an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::02bdd5ca756fbe2e9aafd0e7207e9c79
https://doi.org/10.1016/j.tetlet.2005.01.103
https://doi.org/10.1016/j.tetlet.2005.01.103
Autor:
Pete Yehl, Robert B. Waters, Firoz D. Antia, Fred J. Fleitz, Joseph D. Armstrong, Christopher J. Welch, David J. Mathre, Norihiro Ikemoto
Publikováno v:
Organic Process Research & Development. 8:186-191
Chromatography plays a vital role in supporting preclinical pharmaceutical development, whether in providing assays for purity determinations, preparative separation of small amounts of intermediates for route selection studies, or purification of bu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::807565fbb44b28eb826ca72786955aa9
https://doi.org/10.1021/op0300443
https://doi.org/10.1021/op0300443
Autor:
Jinchu Liu, Norihiro Ikemoto, Joseph D. Armstrong, Naijun Wu, Ralph P. Volante, Robert A. Reamer, Dan Petrillo, Fred J. Fleitz, Peter M. Yehl, Ronald H. Szumigala, Donald R. Gauthier
Publikováno v:
Tetrahedron: Asymmetry. 14:3557-3567
An efficient stereoselective preparation of HIV protease inhibitor (+)-1 was synthesized on multi-kilogram scale in 16 steps without the use of chromatography. The key steps include the diastereoselective alkylation of acetal 3, a diastereoselective
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::07556e6c00e9202b9d45ebac373a6f98
https://doi.org/10.1016/j.tetasy.2003.09.023
https://doi.org/10.1016/j.tetasy.2003.09.023
Publikováno v:
Tetrahedron. 59:1317-1325
A β3 adrenergic receptor agonist was prepared on a multi-kilogram scale in high yield and purity via a convergent synthesis. A key intermediate in this synthesis was an arylthiazolylbenzenesulfonyl chloride. The triaryl segment of this sulfonyl chlo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c20e869df219a9717ecea25e4a13490a
https://doi.org/10.1016/s0040-4020(03)00018-8
https://doi.org/10.1016/s0040-4020(03)00018-8
Autor:
Randolph Greasham, Norihiro Ikemoto, Kodzo Gbewonyo, Christine Chirdo, Barry C. Buckland, Carrie Ann Maxwell, Michel Chartrain, Vanessa Sandford, Jerelyn Osoria, Colleen S. Taylor, Sarah Stahl
Publikováno v:
Journal of Bioscience and Bioengineering. 90:321-327
An attractive method for producing cis-1,2-dihydroxy-3-methylcyclohexa-3,5-diene (toluene cis glycol) was developed employing a cis dihydrodiol dehydrogenase "deficient" strain of Rhodococcus (MA 7249). The toluene cis glycol produced was found to ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84dcf5e0fb116a2ffcd7d9417602ab08
https://doi.org/10.1016/s1389-1723(00)80088-2
https://doi.org/10.1016/s1389-1723(00)80088-2
Asymmetric direduction of 1,2-indanedione to cis (1S,2R) indanediol by Trichosporon cutaneum MY 1506
Publikováno v:
Journal of Bioscience and Bioengineering. 88:495-499
Cis (1 S ,2 R ) indanediol is a potential precursor to (−)- cis (1 S ,2 R )-1-aminoindan-2-ol, a key chiral synthon for a leading HIV protease inhibitor, Crixivan® (Indinavir). A potential route to the biosynthesis of this important precursor, the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aeda8e448a9fbdce4b05c4e52abfee47
https://doi.org/10.1016/s1389-1723(00)87665-3
https://doi.org/10.1016/s1389-1723(00)87665-3