New entry to C2 symmetric trans-2,6-bis(hydroxymethyl)-piperidine derivatives via the Sharpless asymmetric dihydroxylation

This publication has 15 references indexed in Scilit:

• Preparation of Nonracemic 3,5-Disubstituted-.gamma.-butyrolactones: An Effective Sequent Auxiliary for Amide Alkylation and Iodolactonization
  The Journal of Organic Chemistry, 1994
• Synthesis of both enantiomers of C2 symmetric trans-2,5-bis(hydroxymethyl)pyrrolidine. Lipase mediated sequential kinetic resolutions
  Tetrahedron Letters, 1994
• Doubly Diastereoselective Iodolactonizations: Olefin and Face Selectivity in Nona-2,7-diene-5-carboxylic Acid Cyclizations
  The Journal of Organic Chemistry, 1994
• A Convenient Synthesis of Enantiomeric Pairs of 2,5-Disubstituted Pyrrolidines of C₂-Symmetry
  Synthesis, 1993
• Synthesis of enantiomerically pure (2R, 5R) disubstituted pyrrolidines from D-mannitol
  Tetrahedron, 1992
• Enantioselective route to .gamma.-butyrolactones: chiral auxiliary mediated amide alkylation and iodolactonization
  The Journal of Organic Chemistry, 1990
• Synthesis of (2R, 6R)-(−)-2,6-lupetidine: 2,6-disubstituted piperidines as potentially useful “C2-symmetric” chiral reagents.
  Tetrahedron Letters, 1990
• C2 symmetry and asymmetric induction
  Chemical Reviews, 1989
• Asymmetric reactions using C2-symmetrically 2,5-disubstituted pyrrolidines as chiral auxiliaries.
  Journal of Synthetic Organic Chemistry, Japan, 1986
• Asymmetric alkylation of carboxyamides by using trans-2,5-disubstituted pyrrolidines as chiral auxiliaries
  Tetrahedron Letters, 1984