Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Kento Yamazaki"'
Autor:
Yuki Yamamoto, Akihiro Tabuchi, Kazumi Hosono, Takanori Ochi, Kento Yamazaki, Shintaro Kodama, Akihiro Nomoto, Akiya Ogawa
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 17, Iss 1, Pp 2906-2914 (2021)
A simple and efficient method for α-brominating lactones that affords α-bromolactones under mild conditions using tetraalkylammonium hydroxide (R4N+OH−) as a base was developed. Lactones are ring-opened with Br2 and a substoichiometric amount of
Externí odkaz:
https://doaj.org/article/4bdccb111f0545ad8ad5ea5f20007c41
Publikováno v:
Journal of the Japan society of photogrammetry and remote sensing. 60:121-128
Publikováno v:
Bioscience, biotechnology, and biochemistry. 85(9)
Colored compounds formed by the Maillard reaction of carnosine with xylose or glucose were investigated in this study. Yellow pigments showing an absorption maximum at 450 nm were found in a heated solution of carnosine with xylose at pH 5.0. These p
Publikováno v:
GCCE
This paper introduces data communication and flexible data compression methods in SIGMA, the application framework we are developing. Recently, various kinds of wireless communication technologies and sensing devices have been developed. Hence, the o
Publikováno v:
GCCE
This paper describes the design of an application framework for advanced use of spatiotemporal imagery data, and the application developed with our framework. Our framework provides a mechanism to share the data captured from a wide variety of sensor
Autor:
Yoshikazu Kimura, Kouta Adachi, Kento Yamazaki, Katsuya Saito, Masayuki Kirihara, Rie Osugi, Ryoji Matsushima
Publikováno v:
The Journal of organic chemistry. 84(12)
Sodium hypochlorite pentahydrate (NaOCl·5H2O) can be used toward the efficient glycol cleavage of trans-cyclic glycols, which are generally resistant to this transformation. Interestingly, the reaction of cis-cyclic glycols with NaOCl·5H2O is slowe
Autor:
Yoshikazu Kimura, Saori Kitagawa, Yukari Kinoshita, Tomohide Okada, Masayuki Kirihara, Toshiaki Iwai, Hiroaki Matsumuro, Kento Yamazaki
Publikováno v:
Synlett. 26:2547-2552
Oxidation of sulfides with sodium hypochlorite pentahydrate crystals (1.1 equiv) in an aqueous acetonitrile solution selectively produces the corresponding sulfoxides in high yields. This procedure is catalyst-free and environmentally benign.
Autor:
Mari Kishida, Yukari Kinoshita, Toshiaki Iwai, Shiro Yamashoji, Haruka Takeuchi, Yuki Nishimura, Yuki Ishizuka, Takuya Noguchi, Sayuri Naito, Honoka Hanai, Kento Yamazaki, Masayuki Kirihara, Tomomi Ogata
Publikováno v:
Tetrahedron. 70:2464-2471
The reaction of aromatic or benzylic disulfides with 2.5 equiv of Selectfluor™ in acetonitrile/water (10:1) at room temperature efficiently produced the corresponding thiosulfonates. Conversely, the reaction of disulfides with 6.5 equiv of Selectfl
Autor:
Yukihiro Sugiyama, Saori Kitagawa, Yoshikazu Kimura, Tomotake Asawa, Hiroaki Matsumuro, Kento Yamazaki, Tomomi Akiyama, Masayuki Kirihara, Tomohide Okada, Toshiaki Iwai
Publikováno v:
Chemistry Letters. 44:185-187
The reaction of disulfides or thiols with sodium hypochlorite pentahydrate in acetic acid efficiently provided the corresponding sulfonyl chlorides in high yields.
Autor:
Takaya Suzuki, Kento Yamazaki, Satoshi Suzuki, Masayuki Kirihara, Toshiaki Iwai, Yuki Ishizuka, Ryoji Matsushima
Publikováno v:
Tetrahedron Letters. 54:5477-5480
The reaction of dithioacetals with 30% hydrogen peroxide in the presence of catalytic amounts of iron(III) acetylacetonate and sodium iodide efficiently produced the corresponding carbonyl compounds in high yields.