Zobrazeno 1 - 10
of 152
pro vyhledávání: '"Kazuo Fukuzumi"'
Publikováno v:
Journal of Japan Oil Chemists' Society. 27:70-75
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b0f8eb080b526aaf68fbb0f62685c804
https://doi.org/10.5650/jos1956.27.70
https://doi.org/10.5650/jos1956.27.70
Publikováno v:
Journal of Japan Oil Chemists' Society. 24:518-521
Unsolvated Grignard reagents with WCl6 are effective cocatalysts in the olefin metathesis. Activity of WCl6-BuMgI in benzene medium is comparable with those derived from BuLi. The optimum ratio of BuMgI to WCl6 was 2.0, and products of Friedel-Crafts
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b998dc7f9d1c439a88082df86e804521
https://doi.org/10.5650/jos1956.24.518
https://doi.org/10.5650/jos1956.24.518
Publikováno v:
The Journal of Organic Chemistry. 42:431-434
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c6f662bafe4aff2e93be83cbaa2542d
https://doi.org/10.1021/jo00423a008
https://doi.org/10.1021/jo00423a008
Autor:
Nobuo IKEDA, Kazuo FUKUZUMI
Publikováno v:
Journal of Japan Oil Chemists' Society. 27:33-37
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f68486ba1eb62b4c12ddb03e99dd6e9
https://doi.org/10.5650/jos1956.27.33
https://doi.org/10.5650/jos1956.27.33
Publikováno v:
Journal of Catalysis. 39:375-382
The isomerization of 1,5-cyclooctadiene to cis -bicyclo[3.3.0]oct-2-ene, 1,4-cyclooctadiene and 1,3-cyclooctadiene catalyzed by transition metal complexes was studied. Nickel(II) complexes were found to have excellent catalytic activities for the iso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::83b5e644e1bd0993c842c4c502c31287
https://doi.org/10.1016/0021-9517(75)90304-8
https://doi.org/10.1016/0021-9517(75)90304-8
Autor:
Nobuo Ikeda, Kazuo Fukuzumi
Publikováno v:
Journal of the American Oil Chemists’ Society. 54:355-359
The antioxidant effects of ion exchange resins and ethyleneimine polymer on the autoxidation products of methyl linoleate in a heterogeneous reaction system are discussed. Results from analyses of the various autoxidation products from linoleate samp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::491d58745426d3da9ef4f85923279e41
https://doi.org/10.1007/bf02802035
https://doi.org/10.1007/bf02802035
Autor:
Kazuo Fukuzumi, Nobuo Ikeda
Publikováno v:
Journal of the American Oil Chemists Society. 51:340-346
Recently, much literature concerning the effects of NMR shift reagents upon compounds with Lewis’s basic functional groups have been reported. These literatures have shown the effects of NMR shift reagents upon hydroxyl, amino, carbonyl, ether, est
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::81b95470972691c2cfc285bc2434d4ff
https://doi.org/10.1007/bf02632380
https://doi.org/10.1007/bf02632380
Publikováno v:
Journal of Organometallic Chemistry. 193:37-46
When heated with some organic compounds, the triphenylphosphine ligand of RuH 2 (PPh 3 ) 4 , RhH(PPh 3 ) 4 , RuCl 2 (PPh 3 ) 3 , and RhCl(PPh 3 ) 3 were hydrogenolyzed almost completely to benzene and those of PtCl 2 (PPh 3 ) 2 , Pt(PPh 3 ) 4 , and P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d7d84c773279c884f20f7957bf9465f
https://doi.org/10.1016/s0022-328x(00)86074-x
https://doi.org/10.1016/s0022-328x(00)86074-x
Publikováno v:
The Journal of Organic Chemistry. 39:1622-1627
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb506c07568fa3b7bd85b85330e213ab
https://doi.org/10.1021/jo00925a004
https://doi.org/10.1021/jo00925a004
Publikováno v:
Journal of Japan Oil Chemists' Society. 25:136-140
In the homogeneous metathesis of 2-heptene catalyzed by WCl6-Et3Al and WCl6-R4Sn systems, the influence of the reaction medium on the conversion was investigated. Many kinds of halogenated hydrocarbon were found to be the more excellent medium than b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b8d473798f54cda2300bf22b2a975dc
https://doi.org/10.5650/jos1956.25.136
https://doi.org/10.5650/jos1956.25.136