Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Norman L. Holy"'
Autor:
Debra L. Palka, Gary D. Melvin, Travis D. Shepherd, Norman L. Holy, John M. Terhune, Edward A. Trippel
Publikováno v:
Marine Mammal Science. 19:240-243
Autor:
Norman L. Holy, Gary W. Earl, Leung Cheng, Thomas M. Davies, Joseph W. Manthey, Robert C. Kerber, Melvin M. Kestner, Nathan Kornblum, Michael T. Musser
Publikováno v:
The Journal of Organic Chemistry. 52:196-204
Des reactions de substitution faciles et rapides peuvent avoir lieu sur le carbone α du paranitrocumene. Les nucleophiles sont organiques ou non. Les rendements sont eleves et il y a un fort effet sterique. C'est un nouveau moyen de preparation de p
Autor:
Thomas F. Carey, Norman L. Holy
Publikováno v:
Applied Catalysis. 19:219-223
Syngas may be converted to ethanol and n-propanol fairly selectively using tri-metal catalysts of Fe, Co and Rh on silica. Methane is the major byproduct. These catalysts demonstrate high activity at 270°C and 900 psi.
Autor:
Norman L. Holy
Publikováno v:
The Journal of Organic Chemistry. 44:239-243
Autor:
Norman L. Holy, Tay-Yean Lin
Publikováno v:
Journal of Liquid Chromatography. 2:687-695
Evaluation of HPLC as a possible method by which the nitrogen compounds in coal-derived liquids could be analyzed has met with mixed results. Some chromatography fractions display very different HPLC traces in methanol compared with those obtained in
Publikováno v:
Inorganic and Nuclear Chemistry Letters. 13:569-575
Autor:
Norman L. Holy
Publikováno v:
Synthetic Communications. 6:539-542
Methylenedimethylammonium trifluoroacetate and related Mannich reagents have received rather little attention in view of the novel applications conceptually possible for these salts.1 Specifically, these reagents offer two potential advantages to the
Publikováno v:
Journal of the American Chemical Society. 97:5873-5877
Autor:
Norman L. Holy
Publikováno v:
Tetrahedron Letters. 18:3703-3706
Autor:
Norman L. Holy
Publikováno v:
Canadian Journal of Chemistry. 54:1599-1602
Reduction of nitrobenzene with sodium or lithium naphthalenide results in formation of azobenzene and azoxybenzene in modest yields. With sodium naphthalenide, azoxybenzene formation is favored; use of lithium naphthalenide results in enhanced azoben