Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Satoshi Kajita"'
Autor:
Chie Chikara, Satoshi Yoshiura, Satoshi Kajita, Koji Fujikawa, Taishi Imazato, Tadashi Nagasawa
Publikováno v:
2021 IEEE CPMT Symposium Japan (ICSJ).
Publikováno v:
Nishi Nihon Hifuka. 70:423-428
2006年8月の1ヵ月間に当院を受診した全初診患者3234例に足病変のアンケートおよび診察を依頼し, アンケート調査を承諾した16歳以上894例の足病変につき検討した。結果, 足白癬のみ, ある
Autor:
Takashi Kawamura, Masakatsu Ozawa, Yasushi Tsuji, Masahiro Funato, Hiroaki Ogiyama, Satoshi Kajita
Publikováno v:
The Journal of Organic Chemistry. 61:5779-5787
Silylation of allylic acetates (1) using organodisilanes (2) was carried out in the presence of a catalytic amount of Pd(DBA)2−LiCl at 100 °C. The silylation proceeded smoothly without β-hydrogen elimination of a resulting (π-allyl)palladium int
Autor:
Satoshi Kajita, Masahiro Funato, Masakatsu Ozawa, Hiroaki Ogiyama, Takashi Kawamura, Yasushi Tsuji
Publikováno v:
ChemInform. 28
Silylation of allylic acetates (1) using organodisilanes (2) was carried out in the presence of a catalytic amount of Pd(DBA)2−LiCl at 100 °C. The silylation proceeded smoothly without β-hydrogen elimination of a resulting (π-allyl)palladium int
Publikováno v:
ChemInform. 23
The reaction of TeCl4 with lithium amides such as lithium diisopropylamide and N,N-bis(trimethylsilyl)amide followed by treatment with terminal alkynes gives dialkynyl tellurides in moderate to high yields.
Publikováno v:
ChemInform. 23
Two types of tellurium amides have been prepared by the treatment of ArTeI or TeCl4 with LiNR2 in THF, and their reaction with acetylenes gave vinyl tellurides and dialkynyl tellurides.
Publikováno v:
ChemInform. 24
Various allylic acetates (1a-j) are silylated with hexamethyldisilane (Me 3 SiSiMe 3 , 2) in the presence of a catalytic amount of Pd(DBA) 2 and LiCl at 100 o C to afford the corresponding allylic silanes in high yields. In addition, (trimethylsilyl)
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 67:239-242
Two types of tellurium amides have been prepared by the treatment of ArTeI or TeCl4 with LiNR2 in THF, and their reaction with acetylenes gave vinyl tellurides and dialkynyl tellurides.
Autor:
Hajime Iizuka, Akemi Ishida-Yamamoto, A. Takagi, Satoshi Kajita, Hidetoshi Takahashi, Yoshio Hashimoto, Satoshi Nakamura
Publikováno v:
Clinical and Experimental Dermatology. 34:e320-e321
http://dx.doi.org/10.1111/j.1365-2230.2009.03275.x The definitive version is available at www.blackwell-synergy.com
Autor:
Satoshi Kajita, Hideomi Fujita
Publikováno v:
The Proceedings of Conference of Tokai Branch. :335-336