Preparative bioorganic chemistry; 81 efficient enzymatic preparation of (1 R,4 S)-(+)-4-Hydroxy-2-cyclopentenyl Acetate

Takeshi Sugai, Kenji Mori

Research output: Contribution to journalArticlepeer-review

68 Citations (Scopus)


An efficient method for the preparation of (1R,4S)-(+)-4-hydroxy-2-cyclopentenyl acetate, a useful chiral starting material for the synthesis of prostaglandins, is described. A mixture of cis- A nd trans-3,5-diacetoxycyclopentene, readily obtainable on a preparative laboratory scale, was used as the substrate for the hydrolysis with commercially available pig pancreatic lipase (PPL). PPL hydrolyzed the substrate enantioselectively and substrate-selectively, yielding mainly the (+)-cis-monoacetate and trans-diacetate (Method A). The former was recrystallized to give the diastereomerically and optically pure (+)-cis-monoacetate. Ester exchange of cis/trans mixture of the diacetate in an organic solvent using enzymes as batch or flow system was also investigated (Method B). Method A was applicable to 0.25 mol of substrate, and yielded 0.127 mol (18 g, 51%) of optically pure (+)-monoacetate with recycling recovered materials.

Original languageEnglish
Pages (from-to)19-22
Number of pages4
JournalSynthesis (Germany)
Issue number1
Publication statusPublished - 1988
Externally publishedYes

ASJC Scopus subject areas

  • Catalysis
  • Organic Chemistry


Dive into the research topics of 'Preparative bioorganic chemistry; 8<sup>1</sup> efficient enzymatic preparation of (1 R,4 S)-(+)-4-Hydroxy-2-cyclopentenyl Acetate'. Together they form a unique fingerprint.

Cite this