Resolution of cis-4-O-TBS-2-Cyclopenten-1,4-diol

This publication has 12 references indexed in Scilit:

• An improved preparation of highly enantiomerically enriched (R)-(+)-4-tert-butyldimethylsiloxy-2-cyclopenten-1-one
  Tetrahedron Letters, 1996
• Enantioselective synthesis through enzymatic asymmetrization
  Tetrahedron, 1996
• Synthesis of the four possible stereoisomeric 5′-nor carbocyclic nucleosides from one common enantiomerically pure starting material
  Tetrahedron Letters, 1994
• Synthesis of therapeutically useful prostaglandin and prostacyclin analogs
  Chemical Reviews, 1993
• Enzymatic asymmetrization of meso-2-cycloalken-1,4-diols and their diacetates in organic and aqueous media
  Tetrahedron Letters, 1992
• Synthesis of Nucleosides and Related Compounds. Part XXV. The Alkylation of 6-Chloropurine with Alcohols by Mitsunobu Reaction.
  CHEMICAL & PHARMACEUTICAL BULLETIN, 1992
• Lipase-catalyzed transesterification of meso-cyclopentane diols
  Tetrahedron, 1991
• Enzymes in organic synthesis, 4. Investigation of the pancreatin‐catalyzed acylation of cis‐cyclopent‐2‐ene‐1,4‐diol with various trichloroethyl and vinyl Alkanoates
  European Journal of Organic Chemistry, 1991
• Chiral cyclopentanoid building blocks by asymmetric enzymatic hydrolysis
  Tetrahedron Letters, 1989
• Enzymatic hydrolysis of prochiral cis-1,4-diacyl-2-cyc-lopentenediols: preparation of (1S,4R)-and (1R,4S)-4-hydroxy-2-cyclopentenylderivatives, versatile building blocks for cyclopentanoid natural products.
  Tetrahedron Letters, 1984