Ulhas P. Dhokte
Eli Lilly (United States)(US)
Publications by Year
Research Areas
Organoboron and organosilicon chemistry, Asymmetric Synthesis and Catalysis, Asymmetric Hydrogenation and Catalysis, Chemical Synthesis and Reactions, Chemical Synthesis and Analysis
Most-Cited Works
- → Dibutyltin Oxide Catalyzed Selective Sulfonylation of α-Chelatable Primary Alcohols(1999)189 cited
- → Catalytic Regioselective Sulfonylation of α-Chelatable Alcohols: Scope and Mechanistic Insight(2002)155 cited
- → Hydroboration. 85. Synthesis and hydroboration of (-)-2-phenylapopinene. Comparison of mono(2-phenylapoisopinocampheyl)borane with its 2-methyl and 2-ethyl analogs for the chiral hydroboration of representative alkenes(1990)52 cited
- → A novel approach for total synthesis of cryptophycins via asymmetric crotylboration protocol(1998)37 cited
- → Hydroboration. 90. Synthesis of 2-Isobutyl- and 2-Isopropylapopinenes. Rates and Stoichiometry of the Hydroboration of 2-Organylapopinenes with Borane-Methyl Sulfide and Borane-Tetrahydrofuran(1994)24 cited
- → Chiral Synthesis via Organoboranes. 48. Efficient Synthesis of Trans-Fused Bicyclic and Cyclic Ketones and Secondary Alcohols in High Optical Purities via Asymmetric Cyclic Hydroboration with Isopinocampheylchloroborane Etherate(1998)23 cited
- → Hydroboration. 92. Investigation of Practical Methods for the Synthesis of Optically Pure Isopinocampheylchloroborane for the Asymmetric Hydroboration of Representative Prochiral Alkenes(1996)20 cited
- → Hydroboration. 91. Improved Procedure for the Synthesis of Optically Pure Bis-adducts,N,N,N,'N'-Tetramethylethylenediamine.cntdot.2-organylapoisopinocampheylboranes, from the Corresponding 2-Organylapopinenes of Lower Optical Purity. Conversion of These Adducts into 2-Organylapoisopinocampheylboranes, Useful Asymmetric Hydroborating Reagents(1994)19 cited
- → 2-Isopropylapoisopinocampheylborane, an improved reagent for the asymmetric hydroboration of representative prochiral alkenes(1994)18 cited
- → A general, efficient, convenient synthesis of chiral bis(terpenyl)haloborane reagents, valuable for asymmetric synthesis via organoboranes(1996)16 cited