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pro vyhledávání: '"Hilton M. Weiss"'
Autor:
Kim M. Touchette, Hilton M. Weiss
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 2. :1523-1528
The addition of 0.1 M quaternary ammonium bromide to a solution of 20% trifluoroacetic acid in methylene chloride causes a large rate increase in the reaction of non-conjugated alkynes. The initial vinyl bromide product reacts further to provide a mi
Autor:
Hilton M. Weiss, Kim M. Touchette
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 2. :1517-1522
The addition of 0.1 M quaternary ammonium halide to a solution of 20% trifluoroacetic acid in methylene chloride causes a large rate increase in the reaction of simple alkenes leading to a mixture of alkyl halides and trifluoroacetates. The mechanism
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 2. :756-758
The reaction of oct-4-yne with 20% trifluoroacetic acid and a variety of relatively weak nucleophiles in methylene chloride was found to produce a mixture of anion incorporated and solvent incorporated products. The rates of these reactions with a ra
Autor:
Hilton M. Weiss
Publikováno v:
ChemInform. 22
Some novel methyl- and ethyl-substituted dimers of 2,4-diphenylcyclopentadienones have been detected. Their enthalpies- of dimerization have been determined and compared with values calculated by molecular mechanics. The steric demands of this dimeri
Autor:
Kim M. Touchette, Hilton M. Weiss
Publikováno v:
ChemInform. 29
The addition of 0.1 M quaternary ammonium bromide to a solution of 20% trifluoroacetic acid in methylene chloride causes a large rate increase in the reaction of non-conjugated alkynes. The initial vinyl bromide product reacts further to provide a mi
Publikováno v:
Organicbiomolecular chemistry. 1(12)
In a weakly acidic solution, the addition of HBr to 1-phenylprop-1-yne produces predominantly the anti-Markovnikov product. In this paper, we consider five possible explanations for this behavior and conclude that the concerted addition is occurring
Autor:
Hilton M. Weiss
Publikováno v:
Journal of Chemical Education. 87:1355-1356
A vast majority of polar additions of Bronsted acids to alkynes involve a termolecular transition state. With strong acids, considerable positive charge is developed on carbon and Markovnikov addition predominates. In less acidic solutions, however,
Autor:
Hilton M. Weiss
Publikováno v:
Journal of Chemical Education. 85:1218
Autor:
Hilton M. Weiss
Publikováno v:
Journal of Chemical Education. 84:440
Many organic reactions are catalyzed by strong acids or bases that protonate or deprotonate neutral reactants leading to reactive cations or anions that proceed to products. In enzyme reactions, only weak acids and bases are available to hydrogen bon
Publikováno v:
Organic & Biomolecular Chemistry. 1:2148
The reaction of aryl alkynes with dilute methylene chloride solutions of quaternary ammonium bromide and 20% trifluoroacetic acid produces primarily the syn Markovnikov adducts of hydrogen bromide. At moderate concentrations of the bromide, the princ