Synthesis of homochiral α-alkoxystannanes: stereospecific conversion to cembranolide precursors

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

On the use of the O-methylmandelate ester for establishment of absolute configuration of secondary alcohols

Barry M. Trost, John L. Belletire, Stephen A. Godleski et al. · The Journal of Organic Chemistry · 1986 · 576 citations

Natural Sciences, Chemistry, Analytical Chemistry +6

Asymmetric synthesis via axially dissymmetric molecules. 6. Rational designing of efficient chiral reducing agents. Highly enantioselective reduction of aromatic ketones by binaphthol-modified lithium aluminum hydride reagents

Ryōji Noyori, I. Tomino, Yoshifumi Tanimoto et al. · Journal of the American Chemical Society · 1984 · 343 citations

Natural Sciences, Chemistry, Catalysis +11

.alpha.-Alkoxyorganolithium reagents. A new class of configurationally stable carbanions for organic synthesis

W. Clark Still, C. Sreekumar · Journal of the American Chemical Society · 1980 · 276 citations

Natural Sciences, Chemistry, Inorganic Chemistry +4

Nuclear magnetic resonance nonequivalence of diastereomeric esters of .alpha.-substituted phenylacetic acids for the determination of stereochemical purity

James A. Dale, Harry S. Mosher · Journal of the American Chemical Society · 1968 · 144 citations

Natural Sciences, Biochemistry, Chemistry +9