A. V. TEODOROVIC

Chiral synthesis via organoboranes. 38. Selective reductions. 48. Asymmetric reduction of trifluoromethyl ketones by B-chlorodiisopinocampheylborane in high enantiomeric purity

P. Veeraraghavan Ramachandran, A. V. TEODOROVIC, Herbert C. Brown · Tetrahedron · 1993 · 94 citations

Halogenation, Engineering, Selective Reductions +9

Chiral synthesis via organoboranes. 34. Selective reductions. 47. Asymmetric reduction of hindered .alpha.,.beta.-acetylenic ketones with B-chlorodiisopinocampheylborane to propargylic alcohols of very high enantiomeric excess. Improved workup procedure for the isolation of product alcohols

P. Veeraraghavan Ramachandran, A. V. TEODOROVIC, M. V. RANGAISHENVI et al. · The Journal of Organic Chemistry · 1992 · 88 citations

Product Alcoholsp, Engineering, Altmetric Attention Score +11

Selective reductions. 53. Asymmetric reduction of α-fluoromethyl ketones with B-chlorodiisopinocampheylborane and B-isopinocampheyl-9-borabicyclo[3.3.1]nonane. Combined electronic and steric contributions to the enantiocontrol process

P. Veeraraghavan Ramachandran, A. V. TEODOROVIC, Baoqing Gong et al. · Tetrahedron Asymmetry · 1994 · 48 citations

α-Fluoromethyl Ketones, Biochemistry, Natural Sciences +9

Selective reductions. 52. Efficient asymmetric reduction of α-acetylenic α′-fluoroalkyl ketones with either B-chlorodiisopinocampheylborane or B-isopinocampheyl-9-borabicyclo[3.3.1]nonane in high enantiomeric purity. The influence of fluoro groups in such reductions

P. Veeraraghavan Ramachandran, Baoqing Gong, A. V. TEODOROVIC et al. · Tetrahedron Asymmetry · 1994 · 42 citations

Bioorganic Chemistry, Fluoro Groups, Biochemistry +9

B-Chlorodiiso-2-ethylapopinocampheylborane — an extremely efficient chiral reducing agent for the reduction of prochiral ketones of intermediate steric requirements

Herbert C. Brown, P. Veeraraghavan Ramachandran, A. V. TEODOROVIC et al. · Tetrahedron Letters · 1991 · 33 citations

Medicinal Chemistry, Enantioselective Synthesis, Bioorganic Chemistry +10