Zobrazeno 1 - 10
of 15
pro vyhledávání: '"David S. Soriano"'
Publikováno v:
ChemInform. 26
Reduction of functional groups with hydrogen gas is one of the most important reactions in organic chemistry, dating to the first hydrogenation of ethene to ethane reported by Von Wilde in 18741. Indeed, alkenes are generally rapidly hydrogenated, in
Publikováno v:
Journal of Environmental Science and Health . Part A: Environmental Science and Engineering and Toxicology. 27:89-104
Methyl substitution in dibenz[a,h]anthracene leads to isomeric derivatives with distinctly different carcinogenic potencies. Using the elements of Bay Region carbonium ions and the Seybold‐Smith reactivity theory, these differences in carcinogenic
Publikováno v:
Journal of Environmental Science and Health . Part A: Environmental Science and Engineering and Toxicology. 25:277-289
Methyl substitution in benzo[a]pyrene 1 leads to isomeric derivatives with distinctly different carcinogenic potencies. Using the elements of “Bay‐Region”; carbonium ions and Seybold‐Smith reactivity theory, these differences in carcinogenic
Publikováno v:
Synthetic Communications. 25:3263-3265
Reduction of functional groups with hydrogen gas is one of the most important reactions in organic chemistry, dating to the first hydrogenation of ethene to ethane reported by Von Wilde in 18741. Indeed, alkenes are generally rapidly hydrogenated, in
Autor:
David S. Soriano, Jon A. Draeger
Publikováno v:
Journal of Heterocyclic Chemistry. 27:527-529
Huckel molecular orbital calculations and application of Seybold-Smith reactivity theory suggest that the Bay-Region diol epoxide derived from the 8,9,10,11-benzo ring of dibenz[a,h] acridine (1) is the same in reactivity as that of the 1,2,3,4-ring
Autor:
David S. Soriano, Jon A. Draeger
Publikováno v:
Journal of Chemical Education. 72:84
Comparison of total dissolved solids for several samples of water before and after a single, simple distillation.
Autor:
Jon A. Draeger, David S. Soriano
Publikováno v:
Journal of Chemical Education. 70:414
Autor:
David S. Soriano
Publikováno v:
Journal of Chemical Education. 70:332
Example of the Wolff-Kishner reduction procedure suitable for an undergraduate organic lab experiment.
Publikováno v:
Journal of Heterocyclic Chemistry. 17:1389-1392
A number of 1-alkyl-2-carbomethoxy(benzyloxy)-4-methylazetidines have been prepared by reaction of primary amines with α,γ-dibromo esters. Only one isomer was isolated from the reaction mixture. α-Aminolactones can also be obtained as the minor pr
Publikováno v:
Journal of Heterocyclic Chemistry. 19:89-96
Studies of compounds such as 1-cyclohexyl-2-carbomethoxy-4-methylazetidine by H-1 nmr coupling constants, nuclear Overhauser effects, C-13 steric shifts, and N-15 nmr support the revised assignment of configuration for cis/trans isomers in a series o