Preparation of the enantiomers of 1-phenylethan-1,2-diol. Regio- and enantioselectivity of acylase I and Candida antarctica lipases A and B

This publication has 29 references indexed in Scilit:

• Enantiopure derivatives of 1,2-alkanediols: Substrate requirements of lipase B fromCandida antarctica
  Chirality, 2000
• Biocatalysis in Organic Synthesis. 9. Highly Enantioselective Kinetic Resolution of Secondary Alcohols Catalyzed by Acylase.¹
  Synlett, 1997
• Biocatalysis in Organic Synthesis 7. Enantioselective Transesterification Catalyzed by an Acylase: Remarkable Influence of Remote Substitution and the Nature of the Solvent on the Selectivity1
  Synlett, 1996
• Biocatalysis in Organic Synthesis. 6. First Use of an Acylase as Catalyst in the Irreversible Transacylation of Alcohols and Amines: Application to Selective Transformations1
  Synlett, 1995
• Kinetic resolution of acyclic 1,2-diols using a sequential lipase-catalyzed transesterification in organic solvents
  The Journal of Organic Chemistry, 1994
• Enzymatic acylation in the resolution of methyl threo-2-hydroxy-3-(4-methoxyphenyl)-3-(2-X-phenylthio)propionates in organic solvents
  Journal of the Chemical Society, Perkin Transactions 1, 1993
• Chemoselective benzoylations of 1,2-diols. Reactivity comparisons of reagents. Triphenylphosphine-benzoyl peroxide and triphenylphosphine-diethyl azodicarboxylate-benzoic acid
  The Journal of Organic Chemistry, 1988
• Preparation of chiral diphenyl substituted polyether-diester compounds
  The Journal of Organic Chemistry, 1982
• The mechanism of asymmetric hydrogenation. Chiral bis(diphenylphosphino)-α-phenylalkane complexes in catalytic and structural studies
  Journal of the Chemical Society, Perkin Transactions 2, 1982
• 1,2-Bis(diphenylphosphino)-1-phenylethane: a chiral ditertiary phosphine derived from mandelic acid used as a ligand in asymmetric homogeneous hydrogenation catalysts
  The Journal of Organic Chemistry, 1979