Zobrazeno 1 - 10
of 21
pro vyhledávání: '"D. McKeough"'
Autor:
Risa D. Sargent, Alicia D. McKeough
Publikováno v:
The American naturalist. 200(3)
Dioecious plants can exhibit sexual dimorphism across a suite of plant traits, including susceptibility to herbivory and secondary chemistry. One hypothesis is that because of greater costs of reproduction in females, males should grow faster and inv
Publikováno v:
Rubber Chemistry and Technology. 48:790-794
The pre-vulcanization inhibitor activity of a series of N-(substitutedthio)-phthalimides is attributed to thermal cleavage of the N—S bond with formation of phthalimide and the corresponding thiol radical, which subsequently acts as a scavenger for
Autor:
D. McKeough, K. T. Potts
Publikováno v:
Journal of the American Chemical Society. 96:4276-4279
Autor:
D. McKeough, K. T. Potts
Publikováno v:
Journal of the American Chemical Society. 96:4268-4275
Publikováno v:
Rubber Chemistry and Technology. 47:289-302
Spectral characteristics of several known and new N-substituted-p-nitrosoanilines, e.g., Nitrol, of established utility in promoting the bonding between rubber and carbon black are described. A possible mode of action in their enhancement of the bond
Publikováno v:
Rubber Chemistry and Technology. 46:1299-1315
The activities of the various cyclohexyldithio derivatives of thiazoles, benzoxazole and benzimidazole as accelerators may be correlated with their mass spectral fragmentation patterns. Present in the mass spectra are the molecular ions of 2-hydrodis
Autor:
D. Mckeough, K. T. Potts
Publikováno v:
Chemischer Informationsdienst. 5
Autor:
K. T. Potts, D. Mckeough
Publikováno v:
Chemischer Informationsdienst. 5
Autor:
D. Mckeough, K. T. Potts
Publikováno v:
Chemischer Informationsdienst. 4
Bei der Umsetzung des Sarkosins (I) mit dem Acetylen (II) entsteht primar das mesoionische Oxazol (III), das mit (II) zu dem Pyrrol (IV) reagiert.
Autor:
D. Mckeough, K. T. Potts
Publikováno v:
Chemischer Informationsdienst. 3
Die Kondensation des Sydnons (I) mit dem Acetylen (II) ergibt das Pyrazol (III), das mit P2S5 in (IV) ubergefuhrt wird.