Complete asymmetric induction in [1, 2]-wittig rearrangement of a system involving a binaphthol moiety

High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids

Ikuko I. Ohtani, Takenori Kusumi, Yoel Kashman et al. · Journal of the American Chemical Society · 1991 · 3.2K citations

Natural Sciences, Chemistry, Analytical Chemistry +5

Nuclear magnetic resonance enantiomer regents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate, O-methylmandelate, and .alpha.-methoxy-.alpha.-trifluoromethylphenylacetate (MTPA) esters

James A. Dale, Harry S. Mosher · Journal of the American Chemical Society · 1973 · 2.6K citations

Natural Sciences, Chemistry, Nuclear Chemistry +6

Correlation of configuration and fluorine-19 chemical shifts of .alpha.-methoxy-.alpha.-trifluoromethylphenyl acetate derivatives

Glenn R. Sullivan, James A. Dale, Harry S. Mosher · The Journal of Organic Chemistry · 1973 · 504 citations

Natural Sciences, Chemistry, Medicinal Chemistry +8

Stereochemical analysis of totally stereoselective competing [1,2]- and 2,3]-Wittig rearrangements. Inversion at the lithium-bearing carbon atom

Erik Verner, Theodore Cohen · Journal of the American Chemical Society · 1992 · 90 citations

Natural Sciences, Chemistry, Analytical Chemistry +8

[1,2]-Wittig Rearrangement of Acetal Systems: A Highly Stereocontrolled Conversion of <i>O</i>-Glycosides to <i>C</i>-Glycosides

Katsuhiko Tomooka, Hiroshi Yamamoto, Takeshi Nakai · Journal of the American Chemical Society · 1996 · 89 citations

Pharmacy, Chemistry, Analytical Chemistry +9