Index Catalog // ScholarsArchive@OSU

Creator:: Ogba, O. Maduka
Abstract:: In this Dissertation, the mechanism and stereomechanics of complex organocatalysis and reaction processes are disclosed. The technologies and protocols currently being developed and utilized to efficiently investigate these systems using theory are highlighted. A detailed computational study of peptide-catalyzed acylations is disclosed. In particular, the magnitude of all possible non-bonding...
Resource Type:: Dissertation
Full Text:: ., Int. Ed. 2000, 39, 1352.   11 Hajos, Z. G.; Parrish, D. R. J. Org. Chem. 1974, 39, 1615. 12 List, B

Creator:: Hogeland, Jane S.
Resource Type:: Dissertation
Full Text:: me. I would also like to thank Drs. Richard W. Thies, Douglas A. Keszler, W. Curtis Johnson, and

Creator:: Jones, Roger A.
Resource Type:: Masters Thesis
Full Text:: members of my committee, Dr. W. D. Loveland, Prof. J. G. Mingle, Dr. R. A. Schmitt, and Dr. B. I. Spinrad

Creator:: Genualdi, Susan A.
Abstract:: The use of semi-volatile organic compounds (SOCs) as molecular markers to identify the contributions of regional and long-range atmospheric transport, as well as current and historic sources, and contaminant deposition in remote ecosystems of the Western U.S. was investigated. Trans-Pacific air masses influenced by Siberian biomass burning events had elevated...
Resource Type:: Dissertation
Full Text:: ). LITERATURE CITED (1) Bailey, R.; Barrie, L. A.; Halsall, C. J.; Fellin, P.; Muir, D. C. G. Journal of

Creator:: Wu, Zhenhua
Abstract:: Three distinct methods to achieve the stereoselective synthesis of carbon-carbon bonds were investigated, encompassing: (i) the formation of axially chiral biaryl molecules by enantioselective Suzuki cross-coupling, (ii) the synthesis of α-phenylalkylboronic esters by enantioselective chain extension, and (iii) the stereospecific synthesis of alkenes by eliminative cross-coupling of enantioenriched sp³-hybridized carbenoids....
Resource Type:: Dissertation

Creator:: Li, Yang
Abstract:: Irradiation of a tryptamine linked through its side-chain nitrogen to an alkylidene malonate residue results in an intramolecular [2 + 2] cycloaddition to the indole 2,3-double bond. The resultant cyclobutane undergoes spontaneous retro-Mannich fission to produce a spiro[indoline-3,3-pyrrolenine] with relative configuration defined by the orientation of substituents in the transient...
Resource Type:: Dissertation
Full Text:: . Woodward, R. B.; Hoffmann, R. J. Am. Chem. Soc. 1965, 87, 395. 2. Ciamician, G.; Silber. P. Chemische

ScholarsArchive@OSU