Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Norito Uchino"'
Autor:
Norito Uchino, Ken Sasaki, Kikuji Nakao, Kentaro Takagi, Yoshihiko Kobayashi, M. Sakai, Yasumasa Sakakibara
Publikováno v:
ChemInform. 25
The homo-coupling of 1-alkenyl halides was examined in the presence of NiBr2(PPh3)2, PPh3, and excess zinc. The reactions proceed under very mild conditions to give high yields of conjugated dienes. The addition of KI or thiourea was unnecessary for
Publikováno v:
ChemInform. 25
Publikováno v:
Bulletin of the Chemical Society of Japan. 64:2236-2241
The isomerization of 1,5-cyclooctadiene (1,5-COD) with Ni(acac)2–Et3Al2Cl3–phosphorus ligand (Ni : Al2 : P=1 : 10 : 3) was first examined with varying P ligands in toluene in order to find suitable conditions for the formation of 1,4-COD. The pro
Publikováno v:
Bulletin of the Chemical Society of Japan. 66:2776-2778
The cyanation of 3-bromopyridine catalyzed by in situ generated Ni(PPh3)n was examined with various MCN (M = K, Na)-dipolar aprotic solvent systems by four procedures. Under certain reaction conditions, 3-bromopyridine and several heteroaromatic hali
Autor:
Norito Uchino, Kentaro Takagi, Yasumasa Sakakibara, Yoshihiko Kobayashi, M. Sakai, Kikuji Nakao, Ken Sasaki
Publikováno v:
Bulletin of the Chemical Society of Japan. 66:2446-2448
The homo-coupling of 1-alkenyl halides was examined in the presence of NiBr2(PPh3)2, PPh3, and excess zinc. The reactions proceed under very mild conditions to give high yields of conjugated dienes. The addition of KI or thiourea was unnecessary for
Publikováno v:
ChemInform. 21
Publikováno v:
Sen'i Gakkaishi. 33:T325-T331
Publikováno v:
Bulletin of the Chemical Society of Japan. 60:2923-2926
1,4-Cyclohexadiene was hydrogenated selectively to cyclohexene with a nickel catalyst generated from bis(acetylacetonato)nickel(II), triethyldialuminium trichloride, and triphenylphosphine at 40 °C under an atmospheric pressure of hydrogen. The hydr
Publikováno v:
Sen'i Gakkaishi. 34:T551-T556
Publikováno v:
Sen'i Gakkaishi. 38:T304-T311
Polyesters were prepared from the interfacial polycondensation of the following bisphenols with diacid chloride of terephthalic acid or adipic acid; bisphenol-A, tetrachloro or tetrabromobisphenol-A, bisphenol-S, and tetrachloro or tetrabromo bisphen