Highly stereoselective reaction ofα-methylthio aldehydes with allyltriphenylstannane: Synthesis of anti-β-methylthio alcohols

Torsional strain involving partial bonds. The stereochemistry of the lithium aluminium hydride reduction of some simple open-chain ketones

M. CHEREST, Hugh Felkin, Nicole Prudent · Tetrahedron Letters · 1968 · 886 citations

Materials Science, Engineering, Organic Chemistry +5

Stereocontrolled additions of allyltri--butyl-stannane to α-hydroxyaldehyde derivatives. A useful route to monoprotected or diols.

Gary E. Keck, Eugene P. Boden · Tetrahedron Letters · 1984 · 149 citations

Engineering, Useful Route, Organic Chemistry +8

Stereoselective reduction of α-hydroxy ketones

Tadashi Nakata, Tadasu Tanaka, Takeshi Oishi · Tetrahedron Letters · 1983 · 149 citations

Organic Chemistry, Stereoselective Synthesis, Chemistry +3

Acyclic stereoselection. 22. Diastereofacial selectivity in the Lewis acid mediated reactions of allylsilanes with chiral aldehydes and enones

Clayton H. Heathcock, Syun‐ichi Kiyooka, Todd A. Blumenkopf · The Journal of Organic Chemistry · 1984 · 102 citations

Asymmetric Catalysis, Cross-coupling Reaction, Engineering +12

Chemistry of sulfoxides and related compounds. XLIII. Conversion of ketones to epoxides via .beta.-hydroxy sulfides

James R. Shanklin, Carl R. Johnson, Janet Ollinger et al. · Journal of the American Chemical Society · 1973 · 68 citations

Chemical Engineering, Chemical Measurement, Engineering +13