Thomas M. Mitzel

Addition of Allylindium Reagents to Aldehydes Substituted at C_α or C_β with Heteroatomic Functional Groups. Analysis of the Modulation in Diastereoselectivity Attainable in Aqueous, Organic, and Mixed Solvent Systems

Leo A. Paquette, Thomas M. Mitzel · Journal of the American Chemical Society · 1996 · 165 citations

Chemical Engineering, Allylindium Reagents, Engineering +15

Diastereoselection during 1,2-Addition of the Allylindium Reagent to α-Thia and α-Amino Aldehydes in Aqueous and Organic Solvents

Leo A. Paquette, Thomas M. Mitzel, Methvin Isaac et al. · The Journal of Organic Chemistry · 1997 · 85 citations

α-Amino Aldehydes, Enantioselective Synthesis, Engineering +11

Comparative Diastereoselectivity Analysis of Crotylindium and 3-Bromoallylindium Additions to α-Oxy Aldehydes in Aqueous and Nonaqueous Solvent Systems

Leo A. Paquette, Thomas M. Mitzel · The Journal of Organic Chemistry · 1996 · 59 citations

Chemical Engineering, Crotyl Bromide, Engineering +15

Chelation control associated with organometallic addition reactions in water. The high stereoselectivity offered by α- and β-hydroxyl substituents obviates the need for protecting groups

Leo A. Paquette, Thomas M. Mitzel · Tetrahedron Letters · 1995 · 53 citations

Biochemistry, High Stereoselectivity, Natural Sciences +7

Use of α-chlorosulfides in indium promoted CC couplings: easy entry into the stereoselective formation of epoxy alkynes

Gregory Engstrom, Meisha A. Morelli, Carolyn Palomo et al. · Tetrahedron Letters · 1999 · 26 citations