Takeshi Shimizu, Akiomi Yoshihisa, Yuki Kanno, Mai Takiguchi, Akihiko Sato, Shunsuke Miura, Yuichi Nakamura, Hiroyuki Yamauchi, Takashi Owada, Satoshi Abe, Takamasa Sato, Satoshi Suzuki, Masayoshi Oikawa, Takayoshi Yamaki, Koichi Sugimoto, Hiroyuki Kunii, Kazuhiko Nakazato, Hitoshi Suzuki, Shu-ichi Saitoh, and Yasuchika Takeishi Department of Cardiology and Hematology, Fukushima Medical Univers...

Serial changes in proximal urethral function after transurethral balloon laser hyperthermia of the prostate (TUBAL-H) in a canine model Author(s) KUROKAWA, Kohei; SUZUKI, Takanori; SUZUKI, Kazuhiro; FUKABORI, Yoshitatsu; IMAI, Kyoichi; YAMANAKA, Hidetoshi Citation 泌尿器科紀要 (1996), 42(9): 655-661 Issue Date 1996-09 URL http://hdl.handle.net/2433/115807 Right Type Departmental Bulletin Paper Textve...

In this paper by using of Suzuki contraction , we prove a fixed point theorem in the set up of fuzzy metric spaces.We also show that, in some specific cases, the results reduce to Suzuki contraction in fuzzy metric spaces. Finally, one example is presented to verify the effectiveness and applicability of our main results.

Benzo[c]cinnolines, thieno[3,2-c]cinnolines, pyrido[3,2-c]cinnolines and the previously undescribed quinoxalino[6,7-c]cinnoline ring system are conveniently prepared by a short synthetic route comprised of Suzuki coupling, base-catalysed cyclisation and deoxygenation. The use of tandem borylation-Suzuki coupling further extends the scope of this process to include highly substituted benzo[c]cin...

A novel method for the synthesis of trisubstituted oxazoles via a one-pot oxazole synthesis/Suzuki-Miyaura coupling sequence has been developed. One-pot formation of 5-(triazinyloxy)oxazoles using carboxylic acids, amino acids and a dehydrative condensing reagent, DMT-MM, followed by Ni-catalyzed Suzuki-Miyaura coupling with boronic acids provided the corresponding 2,4,5-trisubstituted oxazoles...

Clot retraction is mediated by factor XIII-dependent fibrin-aIIbb3myosin axis in platelet sphingomyelin-rich membrane rafts Kohji Kasahara, Mizuho Kaneda, Toshiaki Miki, Kazuko Iida, Naoko Sekino-Suzuki, Ikuo Kawashima, Hidenori Suzuki, Motoyuki Shimonaka, Morio Arai, Yoshiko Ohno-Iwashita, Soichi Kojima, Mitsuhiro Abe, Toshihide Kobayashi, Toshiro Okazaki, Masayoshi Souri, Akitada Ichinose, an...

A concise and atom-economical Suzuki-Miyaura coupling of trialkyl- and triarylboranes with aryl halides is described. This new protocol represents the first general, practical method that efficiently utilizes peralkyl and peraryl groups of the unactivated trialkyl- and triarylboranes for the Suzuki-Miyaura coupling reaction.

Conditions for the Suzuki-Miyaura coupling of lithium triisopropyl borates are reported, as well as a procedure for a one-pot lithiation, borylation, and subsequent Suzuki-Miyaura coupling of various heterocycles with aryl halides. These borate species are much more stable toward protodeboronation than the corresponding boronic acids and can conveniently be stored on benchtop at room temperature.

Nominal rewriting is a framework of higher-order rewriting introduced in (Fernández, Gabbay & Mackie, 2004; Fernández & Gabbay, 2007). Recently, (Suzuki et al., 2015) revisited confluence of nominal rewriting in the light of feasibility. We report on an implementation of a confluence tool for (non-closed) nominal rewriting, based on (Suzuki et al., 2015) and succeeding studies.