Directed asymmetric reduction of a carbonyl group via a new homochiral boronate ester.

Organoboron compounds in organic synthesis. 4. Asymmetric aldol reactions

Satoru Masamune, Tsuneo Sato, ByeongMoon. Kim et al. · Journal of the American Chemical Society · 1986 · 165 citations

Asymmetric Aldol Reactionssatoru, Altmetric Attention Score, Organic Chemistry +8

Asymmetric synthesis using tartrate ester modified allylboronates. 1. Factors influencing stereoselectivity

William Roush, Lee K. Hoong, Michelle Palmer et al. · The Journal of Organic Chemistry · 1990 · 131 citations

Altmetrics, Engineering, Donut Icon +15

1,6-asymmetric induction in Lewis acid promoted reactions of ε-methoxy- and ε-hydroxy-allylstannanes and aldehydes

John Carey, Eric J. Thomas · Tetrahedron Letters · 1993 · 41 citations

Cross-coupling Reaction, Engineering, Lewis Acid +7

β-boronate carbonyl derivatives: Synthesis and evidence for the intervention of boronate “ate”-complexes in enolate alkylations.

Richard J. Mears, A. WHITING · Tetrahedron · 1993 · 37 citations

β-Boronate Carbonyl Derivatives, Engineering, Enolate Alkylations +6

Keto boronate reduction: a novel method for high 1,3-relative asymmetric induction

Gary A. Molander, Kevin L. Bobbitt, Christopher K. Murray · Journal of the American Chemical Society · 1992 · 28 citations

Engineering, Chemical Analysis, Altmetric Attention Score +16