Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Tsutomu HAYAKAWA"'
Publikováno v:
Nihon Kikai Gakkai ronbunshu, Vol 80, Iss 816, Pp DR0241-DR0241 (2014)
Vibration measurements of a road-wheel were demonstrated using a fiber Bragg grating sensor (FBG sensor) and a flat-belt test machinery. Davis and Kersey's method to measure Bragg wavelength of an FBG sensor was applied in the tests. An assembled whe
Externí odkaz:
https://doaj.org/article/3907e205205741be8aaa4cf307cbd484
Publikováno v:
Bioscience, Biotechnology, and Biochemistry. 72:2716-2722
The in vitro reactivities of astaxanthin toward peroxynitrite were investigated and the reaction products after scavenging with peroxynitrite were analyzed in order to determine the complete mechanism of this reaction. A series of carotenoids, 13-apo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84946203402ca1d778375043a927e0a5
https://doi.org/10.1271/bbb.80358
https://doi.org/10.1271/bbb.80358
Autor:
Hideo Etoh, Tsutomu Hayakawa, Takashi Maoka, Yukimasa Terada, Aditya Kulkarni, Kumiko Ishizuka, Ryo Yoshioka
Publikováno v:
Tetrahedron Letters. 47:3637-3640
The in vitro reactivities of astaxanthin and β-carotene toward peroxynitrite were investigated and the reaction products after scavenging with peroxynitrite were analyzed. A series of carotenoids substituted with nitro group, 14′-s- cis -15′-nit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5230aad8d1cc85d1e59b9583ab04d841
https://doi.org/10.1016/j.tetlet.2006.03.139
https://doi.org/10.1016/j.tetlet.2006.03.139
Publikováno v:
ChemInform. 31
Dimethyl malonate and dibenzoylmethane attacked the C-2 position of the title 3-nitro-2-enopyranosides from the side opposite the anomeric methoxyl group to afford the 3-enopyranosides (SN2′ products). In the case of 2,4-pentanedione and ethyl acet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49fe8f1184ccaf08232ebc3bf6150a77
https://doi.org/10.1002/chin.200047194
https://doi.org/10.1002/chin.200047194
Publikováno v:
Carbohydrate research. 327(4)
Dimethyl malonate and dibenzoylmethane attacked the C-2 position of the title 3-nitro-2-enopyranosides from the side opposite the anomeric methoxyl group to afford the 3-enopyranosides (SN2′ products). In the case of 2,4-pentanedione and ethyl acet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e14a226f2345a9f5e71139dbb477d1e
https://pubmed.ncbi.nlm.nih.gov/10990034
https://pubmed.ncbi.nlm.nih.gov/10990034
Publikováno v:
Transactions of the JSME (in Japanese). 80:DR0241-DR0241
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea5eefb9e294bc0bd7d3e32d976e8a72
https://doi.org/10.1299/transjsme.2014dr0241
https://doi.org/10.1299/transjsme.2014dr0241
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