Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Thomas R. B. Mitchell"'
Publikováno v:
Canadian Journal of Chemistry. 79:655-669
The mono(acetylacetonato) complexes [MCl(O,O'-acac)(η6-arene)] (M = Ru, Os, arene = C6H6, 1,3,5-C6H3Me3, C6Me6; M = Os, arene = 1,2-C6H4Me2, 1,2,3-C6H3Me3), which are formed from [MCl2(η6-arene)]2 and thallium or sodium acetylacetonate, react with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::07bbc18306001534b23e6c9c781af8c6
https://doi.org/10.1139/v01-076
https://doi.org/10.1139/v01-076
Publikováno v:
Organometallics. 14:1000-1007
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::205255998ea65ab2ba46d401a008e64f
https://doi.org/10.1021/om00002a054
https://doi.org/10.1021/om00002a054
Autor:
Terence W. Turney, Thomas R. B. Mitchell, Ian J. McMahon, Wasantha A. Wickramasinghe, Martin A. Bennett, Glen B. Robertson, Lai Yoong Goh
Publikováno v:
Organometallics. 11:3069-3085
Treatment of the various ruthenium(II) salts [Ru(ONO2)(eta-6-1,2-dimethylarene)L2]NO3 and [Ru(O2CCF3)(eta-6-1,2-dimethylarene)L2]PF6 with KO-t-Bu or (Me3Si)2NNa in the presence of a ligand L' gives o-xylylene (o-quinodimethane) complexes of zerovalen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1595d3a6d1b2afbc72e033b352c38d65
https://doi.org/10.1021/om00045a022
https://doi.org/10.1021/om00045a022
Autor:
Thomas R. B. Mitchell
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[10025-97-5] Cl4Ir (MW 334.02) InChI = 1S/4ClH.Ir/h4*1H;/q;;;;+4/p-4 InChIKey = CALMYRPSSNRCFD-UHFFFAOYSA-J (catalyst precursor for the stereoselective reduction of cyclohexanones1-3) Physical Data: decomposes on heating. Solubility: sol cold H2O, al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::854829089997a6dadcb4bcd89d09decb
https://doi.org/10.1002/047084289x.ri050
https://doi.org/10.1002/047084289x.ri050
Autor:
Thomas R. B. Mitchell, Edward A. McIlgorm, John J. Rooney, Valia Amir-Ebrahimi, James Grimshaw
Publikováno v:
Journal of Molecular Catalysis. 27:337-341
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::613644fc00e1b9eae3d98bfeb4589fff
https://doi.org/10.1016/0304-5102(84)85091-9
https://doi.org/10.1016/0304-5102(84)85091-9
Publikováno v:
Journal of the American Chemical Society. 100:906-911
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b4379606bff1af92054ba73f09f1c2a6
https://doi.org/10.1021/ja00471a041
https://doi.org/10.1021/ja00471a041
Autor:
Valla Amir-Ebrahimi, Thomas R. B. Mitchell, Robert Hamilton, Edward A. McIlgorm, John J. Rooney, Manohar V. Kulkarni
Publikováno v:
Journal of Molecular Catalysis. 22:21-26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::34df85e169d44a06deddbdf62f5154d2
https://doi.org/10.1016/0304-5102(83)80082-0
https://doi.org/10.1016/0304-5102(83)80082-0
Publikováno v:
Tetrahedron Letters. 22:4107-4110
Selective catalytic monoalkylation of arylacetonitriles by primary alcohols can be achieved at ≤ 100° using a catalyst prepared in situ from rhodium trichloride, triphenylphosphine and sodium carbonate. RuH 2 (PPh 3 ) 4 is a more effective catalys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::208f2d2da869f22fca4f0dd212ca0348
https://doi.org/10.1016/s0040-4039(01)82078-5
https://doi.org/10.1016/s0040-4039(01)82078-5
Autor:
Alison F. Bean, Thomas R. B. Mitchell, Michael E. Brown, Mohamed A. Mohamed, Samuel G. Mckee, Andrew K. Galwey
Publikováno v:
Reactivity of Solids. 6:187-203
The kinetics of evolution of the main gaseous products (CO2, CO and CH4) of the isothermal decomposition (543–613 K) of nickel malonate, after preliminary dehydration, were studied in greater resolution than was possible previously, through use of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d6194379d802b828de0c7f4322d68a7
https://doi.org/10.1016/0168-7336(88)80060-3
https://doi.org/10.1016/0168-7336(88)80060-3
Publikováno v:
Tetrahedron. 37:4313-4319
Both RhH(CO)PPh3)3 and a catalyst made in situ from RhCl3·3H2O, PPh3 and Na2CO3 catalyse the reaction of a range of aldehydes with simple primary alcohols to give esters together with alcohols formed by reduction of the aldehydes. The proportion of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b86cf50e640f2bca8fce0a3ad4c0ad7f
https://doi.org/10.1016/0040-4020(81)85027-2
https://doi.org/10.1016/0040-4020(81)85027-2