Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Rudolph W. Kluiber"'
Autor:
Gunther S. Fonken, Chittaranjan Raha, Rudolph W. Kluiber, Allen L. McCloskey, William S. Johnson
Publikováno v:
Organic Syntheses
Di-tert-butyl malonate product: di-tert-butyl malonate product: tert-butyl acetate product: tert-butyl chloroacetate product: tert-butyl bromoacetate product: tert-butyl α-chloropropionate product: tert-butyl o-benzoylbenzoate product: di-tert-butyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bd2e4a20f8f7f108828aaee275df9807
https://doi.org/10.1002/0471264180.os034.07
https://doi.org/10.1002/0471264180.os034.07
Autor:
Rudolph W. Kluiber
Publikováno v:
Journal of Chemical Education. 87:367-367
Autor:
Wayne L. Carrick, Lloyd H Wartman, Rudolph W. Kluiber, Bonner Eugene F, Frank M. Rugg, Joseph Smith
Publikováno v:
Journal of the American Chemical Society. 82:3883-3887
Autor:
Rudolph W. Kluiber
Publikováno v:
Journal of Inorganic and Nuclear Chemistry. 30:2737-2741
Several bis[N-hydroxyalkylsalicylaldiminato]copper[II] complexes were observed to decompose thermally to form quantitative yields of 1:1 complexes in which the imine acts as a tridentate ligand. Such 1:1 complexes prepared from N-[3-hydroxypropyl] im
Autor:
Rudolph W. Kluiber, Sandra Kopycinski
Publikováno v:
Journal of Inorganic and Nuclear Chemistry. 30:1891-1897
The co-ordination of a series of meta and para substituted benzaldehydes with nickel acetylacetonate was studied principally by proton magnetic resonance spectroscopy. The data indicate that the interaction is weak and follows a σ+ correlation to th
Publikováno v:
Inorganic Chemistry. 9:1319-1325
Autor:
Rudolph W. Kluiber
Publikováno v:
The Journal of Organic Chemistry. 30:2037-2041
Autor:
Rudolph W. Kluiber
Publikováno v:
Inorganic Chemistry. 4:1047-1051
Publikováno v:
Journal of Coordination Chemistry. 3:39-45
The exchange rates of various substituted pyridines coordinated with a bis-(β-diketonato)nickel(II) complex and the corresponding uncomplexed ligands are first order over a wide ligand concentration range. They decrease slightly in nonpolar solvents
Publikováno v:
Journal of the American Chemical Society. 87:5350-5356