Expeditious Synthesis of Enantiomerically Pure trans -4,5-Dihydroxy-2-cyclopenten-1-one

Koji Toyama, Satoru Iguchi, Tohru Oishi, Masahiro Hirama

Research output: Contribution to journalArticle

17 Citations (Scopus)

Abstract

A short-step synthesis of (-)-(4R,5S)- and (+)-(4S,5R)-trans-4,5-dihydroxy-2-cyclopenten-1-one derivatives (14) has been achieved via the enzymatic asymmetric transformations of meso-3,4,5-trans,trans-trihydroxycyclopentene derivatives 12 and 15, respectively.

Original languageEnglish
Pages (from-to)1243-1244
Number of pages2
JournalSynlett
Volume1995
Issue number12
DOIs
Publication statusPublished - Dec 1995

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Derivatives
cyclopentenone

All Science Journal Classification (ASJC) codes

  • Organic Chemistry

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Expeditious Synthesis of Enantiomerically Pure trans -4,5-Dihydroxy-2-cyclopenten-1-one. / Toyama, Koji; Iguchi, Satoru; Oishi, Tohru; Hirama, Masahiro.

In: Synlett, Vol. 1995, No. 12, 12.1995, p. 1243-1244.

Research output: Contribution to journalArticle

Toyama, Koji ; Iguchi, Satoru ; Oishi, Tohru ; Hirama, Masahiro. / Expeditious Synthesis of Enantiomerically Pure trans -4,5-Dihydroxy-2-cyclopenten-1-one. In: Synlett. 1995 ; Vol. 1995, No. 12. pp. 1243-1244.
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