Enzymes in organic synthesis: remarkable influence of a π system on the enantioselectivity in PPL catalysed monohydrolysis of 2-substituted 1,3-diacetoxypropanes.

This publication has 21 references indexed in Scilit:

• Enzymes as selective reagents in organic synthesis: Enantioselective preparation of “asymmetrized tris (hydroxymethyl)methane”
  Tetrahedron Letters, 1989
• Enhanced and reversed enantioselectivity of enzymic hydrolysis by simple substrate modifications: the case of 3-hydroxyglutarate diesters
  The Journal of Organic Chemistry, 1988
• Enantioselective hydrolysis of dialkyl 3-monosubstituted glutarates with pig liver esterase: Structure-optical purity relationships
  Tetrahedron Letters, 1988
• Enantiomerenreine glycerin-derivate durch enzymatische hydrolyse prochiraler ester 1)
  Tetrahedron Letters, 1987
• Synthesis of both enantiomeric forms of 2-substituted 1,3-propanediol monoacetates starting from a common prochiral precursor, using enzymatic transformations in aqueous and in organic media
  Tetrahedron Letters, 1986
• Enzymatic differentiation of the enantiotopic hydroxymethyl groups of glycerol; synthesis of chiral building blocks
  Journal of the Chemical Society, Chemical Communications, 1986
• Enantioselective hydrolysis of cis -1,2-diacetoxycycloalkanedimethanols:enzymatic preparation of chiral building blocks from prochiral meso -substrates.
  Tetrahedron Letters, 1985
• Bifunctional chiral synthons via biochemical methods, 4. Chiral precursors to (+)-biotin and (−)-a-factor.
  Tetrahedron Letters, 1984
• Stereochemical control in yeast reduction
  Tetrahedron Letters, 1984
• Stereochemical control of yeast reductions. 1. Asymmetric synthesis of L-carnitine
  Journal of the American Chemical Society, 1983