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

Koji Toyama; Satoru Iguchi; Tohru Oishi; Masahiro Hirama

doi:10.1055/s-1995-5261

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 journal › Article › peer-review

18 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 language	English
Pages (from-to)	1243-1244
Number of pages	2
Journal	Synlett
Volume	1995
Issue number	12
DOIs	https://doi.org/10.1055/s-1995-5261
Publication status	Published - Dec 1995
Externally published	Yes

All Science Journal Classification (ASJC) codes

Organic Chemistry

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10.1055/s-1995-5261

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

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.",

author = "Koji Toyama and Satoru Iguchi and Tohru Oishi and Masahiro Hirama",

year = "1995",

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doi = "10.1055/s-1995-5261",

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AU - Oishi, Tohru

AU - Hirama, Masahiro

PY - 1995/12

Y1 - 1995/12

N2 - 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.

AB - 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.

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U2 - 10.1055/s-1995-5261

DO - 10.1055/s-1995-5261

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JF - Synlett

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ER -

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

Abstract

All Science Journal Classification (ASJC) codes

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