JPS6475479A - Optically active 2,3,4,5,6-pentafluorostyrene oxide - Google Patents

Optically active 2,3,4,5,6-pentafluorostyrene oxide

Info

Publication number
JPS6475479A
JPS6475479A JP23349787A JP23349787A JPS6475479A JP S6475479 A JPS6475479 A JP S6475479A JP 23349787 A JP23349787 A JP 23349787A JP 23349787 A JP23349787 A JP 23349787A JP S6475479 A JPS6475479 A JP S6475479A
Authority
JP
Japan
Prior art keywords
pentafluorostyrene
optically active
oxide
pentafluorostyrene oxide
nocardia
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP23349787A
Other languages
Japanese (ja)
Other versions
JPH0422911B2 (en
Inventor
Keiji Furuhashi
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Eneos Corp
Original Assignee
Nippon Mining Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Nippon Mining Co Ltd filed Critical Nippon Mining Co Ltd
Priority to JP23349787A priority Critical patent/JPS6475479A/en
Publication of JPS6475479A publication Critical patent/JPS6475479A/en
Publication of JPH0422911B2 publication Critical patent/JPH0422911B2/ja
Granted legal-status Critical Current

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  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Epoxy Compounds (AREA)

Abstract

NEW MATERIAL:A compound shown by formula I (C* is asymmetric carbon atom.). USE:Having optical activity and useful as a synthetic raw material for performed chemical mediator such as a drug. PREPARATION:2,3,4,5,6-Pentafluorostyrene is aerobically treated with a bacterium (e.g. Nocardia corallina FERM P-4094) belonging to the genus Nocardia, capable of producing epoxide to give 2,3,4,5,6-pentafluorostyrene oxide. The reaction is preferably carried out at pH 5-9 at 20-50 deg.C for half a day-6 days.
JP23349787A 1987-09-17 1987-09-17 Optically active 2,3,4,5,6-pentafluorostyrene oxide Granted JPS6475479A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP23349787A JPS6475479A (en) 1987-09-17 1987-09-17 Optically active 2,3,4,5,6-pentafluorostyrene oxide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP23349787A JPS6475479A (en) 1987-09-17 1987-09-17 Optically active 2,3,4,5,6-pentafluorostyrene oxide

Publications (2)

Publication Number Publication Date
JPS6475479A true JPS6475479A (en) 1989-03-22
JPH0422911B2 JPH0422911B2 (en) 1992-04-20

Family

ID=16955947

Family Applications (1)

Application Number Title Priority Date Filing Date
JP23349787A Granted JPS6475479A (en) 1987-09-17 1987-09-17 Optically active 2,3,4,5,6-pentafluorostyrene oxide

Country Status (1)

Country Link
JP (1) JPS6475479A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19931779A1 (en) * 1999-07-08 2001-01-18 Guenther Koerber Method for producing connections between unknown radiotelephone owners enables road-users to send and receive coded telephone details by using a display or signals

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19931779A1 (en) * 1999-07-08 2001-01-18 Guenther Koerber Method for producing connections between unknown radiotelephone owners enables road-users to send and receive coded telephone details by using a display or signals

Also Published As

Publication number Publication date
JPH0422911B2 (en) 1992-04-20

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