KR900003103A - 살균제 조성물 - Google Patents

살균제 조성물 Download PDF

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KR900003103A
KR900003103A KR1019890012357A KR890012357A KR900003103A KR 900003103 A KR900003103 A KR 900003103A KR 1019890012357 A KR1019890012357 A KR 1019890012357A KR 890012357 A KR890012357 A KR 890012357A KR 900003103 A KR900003103 A KR 900003103A
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하워드 브리너 풀
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오노 알버어스
셀 인터나쵸 나아레 레사아치 마아츠샤피 비이부이
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Priority claimed from GB888820599A external-priority patent/GB8820599D0/en
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Abstract

내용 없음

Description

살균제 조성물
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (15)

  1. 담체 및 활성 성분으로서, 하기 일반식(I)의 화합물로 구성된 살균제 조성물;
    상기식에서, n은 0-5정수를 나타내고, 각각의 R은 할로겐 원자, 니트로, 시아노, 히드록시, 알킬, 할로알킬, 알콕시, 할로알콕시, 아미노, 알킬아미노, 디알킬 아미노, 알콕시카르보닐, 카르복실, 알카노일, 알킬티오, 알킬설피닐, 알킬설포닐, 카르바모일, 알킬아미도, 시클로알킬 또는 페닐기를 나타내고, R1및 R2는 각각 수소원자 또는 알킬기를 나타내고, R5는 수소 원자 또는 알킬 또는 시클로알킬 기를 나타낸다.
  2. 담체 및 활성성분으로서, 하기 일반식(Ⅱ)의 화합물로 구성된 살균제 조성물;
    상기식에서, n,R,R1,R2및 R5는 제1항에서 정의한 바와 같다.
  3. 담체 및 활성 성분으로서, 하기 일반식(Ⅲ)의 화합물로 구성된 살균제 조성물;
    상기식에서, n,R,R1및 R2는 제1항에서와 같고, X 및 Y는 각각 할로겐 원자를 나타낸다.
  4. 담체 및 활성 성분으로서, 하기 일반식(Ⅵ)의 화합물로 구성된 살균제 조성물;
    상기식에서, n,R,R1및 R2는 제1항에서 정의한 바와 같다.
  5. 담체 및 활성 성분으로서, 하기 일반식(Ⅶ)의 화합물로 구성된 살균제 조성물;
    상기식에서, n,R,R1및 R2는 제1항에서 정의한 바와 같고 R4는 알킬기를 나타낸다.
  6. 제2항, 제3항 및 제4항중 어느 한 항에서 정의된 일반식(Ⅱ),(Ⅲ) 또는 (Ⅵ)의 화합물.
  7. n,R,R1R2및 R5가, n은 0이고 R1및 R2모두가 수소원자를 나타낼때, R5는 수소원자 또는 메틸 기를 나타내지 않는 것을 조건으로하는, 제1항에서 정의된 일반식(I)의 화합물.
  8. n,R,R1R2및 R4가, n이 1이고 R1및 R2모두가 수소원자를 나타내고, R4가 메틸기를 나타낼때, R은 페닐고리의 4-위치에서 치환된 염소 또는 브롬원자를 나타내지 않고, n이 0이고 R1및 R2모두가 메틸기를 나타낼때, R4는 에틸기를 나타내지 않는 것을 조건으로하는, 제5항에서 정의된 것인 일반식(Ⅶ)의 화합물.
  9. 제1항 내지 제5항중 어느 한 항에서 정의된 조성물 또는 제6항 내지 제8항 중 어느 한 항에서 정의된 일반식(I),(Ⅱ),(Ⅲ),(Ⅵ)또는 (Ⅶ)의 화합물로 처리해야 할 장소를 처리하는 것으로 구성된 그 장소에서 균류를 구제하는 방법.
  10. 제1항 내지 제5항중 어느 한항에서 정의된 조성물 또는 제6항 내지 제8항중 어느 한항에서 정의된 일반식(I),(Ⅱ),(Ⅲ),(Ⅵ) 또는 (Ⅶ)의 화합물의 살균제로서의 용도.
  11. 극성 용매의 존재하에서, 하기 일반식(Ⅳ)의 화합물과 하기 일반식(Ⅱ) 또는 (Ⅲ)의 화합물을 가열시킴으로 구성된, 제7항에서 정의된 일반식(I)의 화합물의 제조방법;
    상기식에서, n,R,R1R2및 R5는 제7항에서 정의된 것이고, X 및 Y는 제3항에서 정의된 것이다.
    MOR5(Ⅳ)
    상기식에서, R5는 제1항에서 정의된 것이고, M은 알카리 금속 원자를 나타낸다.
  12. 하기 일반식(Ⅴ)의 용매가 존재하는 가운데, 하기 일반식(Ⅳ)의 화합물과 하기 일반식(Ⅲ)의 화합물을 반응시킴으로 구성된, 제6항에서 정의된 일반식(Ⅱ)의 화합물의 제조방법:
    상기식에서, n,R,R1및 R2는 제1항에서 정의된 것이고, X 및 Y는 제3항에서 정의된 것이다;
    MOR5(Ⅳ)
    상기식에서, R5는 제1항에서 정의된 것이고, M은 제11항에서 정의된 것이다;
    R5OH (Ⅴ)
    상기식에서, R5는 제1항에서 정의된 것이다.
  13. 화합물 XY(여기서, X 및 Y는 제3항에서 정의됨)와, 하기 일반식(Ⅵ)의 화합물을 반응시킴으로 구성된, 제6항에서 정의된 일반식(Ⅲ)의 화합물의 제조 방법:
    상기식에서, n,R,R1및 R2는 제1항에서 정의된 것이다.
  14. 환원제와 하기 일반식(Ⅶ)의 화합물을 반응시키고, 이어 반응 혼합물을 가수분해 시키는 것으로 구성된, 일반식(Ⅵ)의 화합물의 제조방법:
    상기식에서, n,R,R1및 R2는 제1항에서 정의된 것이고, R4는 제5항에서 정의된 것이다.
  15. 산의 존재하에서, 하기 일반식(Ⅸ)의 첫번째 화합물과 하기 일반식(Ⅷ)의 화합물의 반응으로 구성된 제8항에서 정의된 일반식(Ⅶ)의 화합물의 제조방법 및 만일 원한다면 얻어진 일반식(Ⅶ)의 화합물을 산의 존재하에서 일반식(Ⅸ)의 두번째 다른 화합물과의 반응에 의해 일반식(Ⅶ)의 또다른 화합물로 전환시키는 방법:
    상기식에서, n,R,R1및 R2는 제8항에서 정의된 것이다;
    R4OH(Ⅸ)
    상기식에서, R4는 제8항에서 정의된 것이다.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019890012357A 1988-08-31 1989-08-29 살균제 조성물 KR0145712B1 (ko)

Applications Claiming Priority (18)

Application Number Priority Date Filing Date Title
GB888820597A GB8820597D0 (en) 1988-08-31 1988-08-31 Cyclohexanedione derivatives
GB8820601.6 1988-08-31
GB8820600.8 1988-08-31
GB888820602A GB8820602D0 (en) 1988-08-31 1988-08-31 Cyclopentane derivatives
GB888820600A GB8820600D0 (en) 1988-08-31 1988-08-31 Dihalocyclohexanone derivatives
GB8820598.4 1988-08-31
GB888820598A GB8820598D0 (en) 1988-08-31 1988-08-31 Cyclohexanone derivatives
NL8820602.4 1988-08-31
GB888820601A GB8820601D0 (en) 1988-08-31 1988-08-31 Cyclopentane derivatives
NL8820597.6 1988-08-31
GB8820599.2 1988-08-31
NL8820598.4 1988-08-31
GB8820597.6 1988-08-31
NL8820601.6 1988-08-31
GB8820602.4 1988-08-31
NL8820600.8 1988-08-31
GB888820599A GB8820599D0 (en) 1988-08-31 1988-08-31 Cyclohexanone derivatives
NL8820599.2 1988-08-31

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KR900003103A true KR900003103A (ko) 1990-03-23
KR0145712B1 KR0145712B1 (ko) 1998-08-17

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JP (1) JP2852941B2 (ko)
KR (1) KR0145712B1 (ko)
BR (1) BR8904339A (ko)
CA (1) CA1335294C (ko)
DE (1) DE68910907T2 (ko)

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US5262543A (en) * 1988-08-31 1993-11-16 Kureha Kagaku Kogyu Kabushiki Kaisha Process for the preparation of cyclopentane derivatives
GB2225006B (en) * 1988-08-31 1992-02-12 Shell Int Research Process for the preparation of cyclopentane derivatives
US5200535A (en) * 1990-09-03 1993-04-06 Shell Research Limited Cyclohexanone derivatives

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FR1084390A (fr) * 1952-07-22 1955-01-19 Pittsburgh Plate Glass Co Perfectionnements relatifs aux cyclopenténylphénols

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DE68910907D1 (de) 1994-01-05
JPH02131445A (ja) 1990-05-21
EP0358259B1 (en) 1993-11-24
KR0145712B1 (ko) 1998-08-17
US5047426A (en) 1991-09-10
JP2852941B2 (ja) 1999-02-03
EP0358259A1 (en) 1990-03-14
CA1335294C (en) 1995-04-18
BR8904339A (pt) 1990-04-17
DE68910907T2 (de) 1994-03-24

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