Uday S. Racherla

Chiral synthesis via organoboranes. 27. Remarkably rapid and exceptionally enantioselective (approaching 100% ee) allylboration of representative aldehydes at -100.degree. under new, salt-free conditions

Uday S. Racherla, Herbert C. Brown · The Journal of Organic Chemistry · 1991 · 356 citations

Halogenation, Salt-free Conditions, Enantioselective Synthesis +13

Efficient manganese catalysts for low-temperature bleaching

Ronald Hage, Jan E. Iburg, Judith L. Kerschner et al. · Nature · 1994 · 335 citations

Chemical Engineering, Catalytic Application, Engineering +5

Organoboranes. 53. A high-field variable-temperature proton and boron-11 NMR study of the effects of solvent and structure on reactivity in allylboration

Herbert C. Brown, Uday S. Racherla, Perry J. Pellechia · The Journal of Organic Chemistry · 1990 · 130 citations

Chemical Engineering, Molecular Sciences, High-field Variable-temperature Proton +13

Chiral synthesis via organoboranes. 24. B-allylbis(2-isocaranyl)borane as a superior reagent for the asymmetric allylboration of aldehydes

Herbert C. Brown, Ramnarayan S. Randad, K. S. BHAT et al. · Journal of the American Chemical Society · 1990 · 123 citations

Asymmetric Allylboration, Engineering, Biochemistry +12

Organoboranes. 44. A convenient, highly efficient synthesis of triorganylboranes via a modified organometallic route

Herbert C. Brown, Uday S. Racherla · The Journal of Organic Chemistry · 1986 · 108 citations

Novel Organocatalysts, Engineering, Biochemistry +10