Zobrazeno 1 - 10
of 85
pro vyhledávání: '"Masumi Itazaki"'
Publikováno v:
Molecules, Vol 29, Iss 4, p 757 (2024)
The reaction of molybdenum complexes with a tris(pyrazolyl)borate ligand (Et4N[TpMo(CO)3] and Et4N[Tp*Mo(CO)3] (Tp = hydridotris(pyrazolyl)borate, Tp* = hydridotris(3,5-dimethylpyrazolyl)borate)) and InBr3 at a 1:1 molar ratio afforded molybdenum–i
Externí odkaz:
https://doaj.org/article/8619a54afde44be68b8b207d0c4241b6
Autor:
Masumi Itazaki, Kento Okabayashi, Takanari Matsutani, Tomoya Nochida, Toshiyuki Moriuchi, Hiroshi Nakazawa
Publikováno v:
Molecules, Vol 27, Iss 17, p 5564 (2022)
Reactions of isocyanates/isothiocyanates with primary and secondary phosphines without solvent at room temperature afforded phosphinecarboxamide/phosphinecarbothioamide, respectively, in excellent yields. Furthermore, palladium complex Pd(COD)Cl2 was
Externí odkaz:
https://doaj.org/article/f2689e7e024a4e92b82e844cd2908111
Selective Double Addition Reaction of an E‒H Bond (E = Si, B) to a C≡N Triple Bond of Organonitriles
Autor:
Masumi Itazaki, Hiroshi Nakazawa
Publikováno v:
Molecules, Vol 23, Iss 11, p 2769 (2018)
The catalytic double hydrometalation such as hydrosilylation and hydroborylation of organonitriles has attracted considerable attention because the obtained products are widely used in organic synthesis and it is thought to be one of the effective me
Externí odkaz:
https://doaj.org/article/ec5ceac0a6f64aa29da870d68130d170
Publikováno v:
Acta Crystallographica Section E, Vol 64, Iss 12, Pp m1578-m1578 (2008)
In the title complex, [Fe(C5H5){Sn(C2H5)3}(C5H5N)(CO)], the Fe atom is coordinated by carbonyl, pyridine, triethylstannyl and cyclopentadienyl ligands in a typical three-legged piano-stool configuration. The Fe—Sn and Fe—N bond distances are 2.54
Externí odkaz:
https://doaj.org/article/48ccd2772a444f4e98e4ba75058c6ad5
Publikováno v:
Chemical Communications. 56:443-445
Reactions of isocyanates with primary and secondary phosphines without solvent at room temperature afforded the corresponding phosphinecarboxamide (RN(H)COPR'2) in excellent yields. This reaction system is applicable for isothiocyanates. The compound
Autor:
Hiroshi Nakazawa, Masumi Itazaki
Publikováno v:
Journal of Synthetic Organic Chemistry, Japan. 77:220-226
Autor:
Susumu Kawauchi, Masahiro Miura, Tomoaki Hinoue, Yoshihiro Hayashi, Hiroshi Nakazawa, Yoshinosuke Usuki, Shintaro Yamane, Tetsuya Satoh, Masumi Itazaki
Publikováno v:
Chemistry - A European Journal. 24(31):7852-7855
The iridium(III)/copper(II)-catalyzed dehydrogenative coupling of salicylaldehydes with internal alkynes proceeds efficiently under atmospheric oxygen through aldehyde C-H bond cleavage and decarbonylation. A variety of benzofuran derivatives can be
Publikováno v:
Bulletin of the Chemical Society of Japan. 91:588-593
A silyl-tethered dihydride iron complex was synthesized by photolysis of a monohydride iron complex bearing a pendant hydrosilyl group. The coordination mode of the two hydrides and the tethered silyl ligand was investigated by 1H NMR spectroscopy an
Publikováno v:
Inorganic Chemistry. 56(22):13709-13714
Organonitriles (RC≡N) were selectively converted into the corresponding diborylamines (RCH2N(Bpin)2) in reactions with pinacolborane (pinBH) in the presence of a catalytic amount of the iron–indium complex [Fe(CH3CN)6][cis-Fe(CO)4(InCl3)2]. The c
Publikováno v:
Journal of Organometallic Chemistry. 847:251-257
An iron methyl complex Cp*(CO)2Fe(Me) reacts with silylferrocene HSiR2Fc (Fc = C5H4FeC5H5, R = Me, Ph) to afford the iron complex with a ferrocenylsilyl ligand, Cp*(CO)2Fe(SiR2Fc) (R = Me: 1, Ph: 2). On the other hand, the reactions of a ruthenium me