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      광학활성 제초제 fenoxaprop-p-ethyl [ethyl (R)-2-{4-(6-chloro-1,3-benzoxazol-2-yloxy)phenoxy}propionate]의 새로운 합성법

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      https://www.riss.kr/link?id=A76192416

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      다국어 초록 (Multilingual Abstract)

      Fenoxaprop-p-ethyl[Ethyl (R)-2-{4-(6-chloro-1,3-benzoxazol- 2-yloxy)phenoxy}propionate] is well known as a herbicide for its specific activity against the weed grasses. This compound was synthesized by the reaction of 4-(6-chloro-1,3-benzoxazol-2-ylox...

      Fenoxaprop-p-ethyl[Ethyl (R)-2-{4-(6-chloro-1,3-benzoxazol- 2-yloxy)phenoxy}propionate] is well known as a herbicide for its specific activity against the weed grasses. This compound was synthesized by the reaction of 4-(6-chloro-1,3-benzoxazol-2-yloxy)phenol and ethyl (S)-O-(p-toluenesulfonyl)lactate in good yields with high optical pure (optical purity : 99.9% up). In this process Walden inversion occurs, whereby the S-configuration of the propionic acid derivative is converted to the R-configuration of the final product. 4-(6-Chloro-1,3-benzoxazol-2-yloxy)phenol was obtained by 5 step reactions in over-all 70% yields using inexpensive raw materials.

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      참고문헌 (Reference)

      1 "propionic acid by enzymic hydrolysis of its racemic esters" Kazutaka Ari 4-hydroxyphe (4-hydroxyphe): 1986

      2 "The Analgestic Activity of Some Benzoxazolone Derivatives" 1265-1268, 1949

      3 "Synthesis and Herbicidal Activity of N" 1 1008-1010, 1975

      4 "Regioselectivity in the C-acylation of 2" 6649-6654, 1991

      5 "Process for the preparation of 2-mercaptobenzoxazoles" -4, 1987

      6 "Process for the preparation of 2-mercaptobenzoxazoles" -4, 1984

      7 "Process for the Production of Heterocyclic Substituted Oxyphenoxyalkanoic acid Derivatives" 1981

      8 "Process for the Production of Benzimidazolyl" -3, 1985

      9 "Process for the Production of 2-Mercaptobenzimidazoles" 1992

      10 "Process for the Preparation of Heterocyclic Phenyl Ethers" -4, 1986

      1 "propionic acid by enzymic hydrolysis of its racemic esters" Kazutaka Ari 4-hydroxyphe (4-hydroxyphe): 1986

      2 "The Analgestic Activity of Some Benzoxazolone Derivatives" 1265-1268, 1949

      3 "Synthesis and Herbicidal Activity of N" 1 1008-1010, 1975

      4 "Regioselectivity in the C-acylation of 2" 6649-6654, 1991

      5 "Process for the preparation of 2-mercaptobenzoxazoles" -4, 1987

      6 "Process for the preparation of 2-mercaptobenzoxazoles" -4, 1984

      7 "Process for the Production of Heterocyclic Substituted Oxyphenoxyalkanoic acid Derivatives" 1981

      8 "Process for the Production of Benzimidazolyl" -3, 1985

      9 "Process for the Production of 2-Mercaptobenzimidazoles" 1992

      10 "Process for the Preparation of Heterocyclic Phenyl Ethers" -4, 1986

      11 "Process for the Manufacture of 2" 6 6-4, 1984

      12 "Process for Preparing 2-Chlorobenzoxazoles" -4, 1985

      13 "Process for Preparing 2-Chlorobenzo thiazoles and 2-Chlorobenzoxazoles" 5 : 502-201, 1996

      14 "Process for Preparation of 2" 6-4, 1987

      15 "Prepn of 6-chloro-2- mercaptobenzoxazide-by reaction of 5-chloro-2- aminophenol with carbon disulfide in aq soln" 1994

      16 "Preparation of (R)-2-(4- Hydroxyphenoxy)propionic acid by biotransformation" 46 (46): 33-35, 1996

      17 "Method for Producing Chlorobenzoxazolene" 6 : 274-739, 2001

      18 "Lipase isozymes for stereoselective hydrolysis of esters or transesterification" 1990

      19 "In Bioorganic Chemistry of Pesticide" Inc p-aryloxyphe (p-aryloxyphe): 501-518, 1985

      20 "Herbicidal Phenoxypropionic Acid N-Alkyl-N-2-fluorophenyl Amide Compounds" 2000

      21 "Herbicidal Esters of D-1-" phe (phe): -4, 1985

      22 "Facile Rearrangements of Alkynylamino Heterocycles with Noble Metal Cations" 61 : 3289-3297, 1996

      23 "Composition and Method for Relieving Spasticity" 1959

      24 "Chromo- genic Lactate Leukocyte Esterase Substrates" 8 : 76-80, 1997

      25 "Carbo- nylation of o-Phenylenediamine and o-Aminophenol with Dimethyl Carbonate Using Lead Compounds as Catalysts" 197 : 91-97, 2001

      26 "Benzthiazole or Benzoxazole Ethers" -4, 1983

      27 "Asymmetric Synthesis of Chiral Secondary Alcohols" 5 : 629-423, 1997

      28 "An Improved Method for the Synthesis of 2-Thioxo-2" 3 3 936-937, 1983

      29 "An Improved Method for the Halogenation of 2" 275-278, 1991

      30 "A Simple Synthesis of 2" 19911937-1939

      31 "A New 5-HT3 Receptor Ligand. II. Structure-Activity Analysis of 5-HT3 Receptor Agonist Action in the Gut" 46 (46): 445-451, 1996

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      연구자 네트워크맵

      공동연구자 (7)

      유사연구자 (20) 활용도상위20명

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2027 평가예정 재인증평가 신청대상 (재인증)
      2021-01-01 평가 등재학술지 유지 (재인증) KCI등재
      2018-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2015-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2011-01-01 평가 등재 1차 FAIL (등재유지) KCI등재
      2008-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2007-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2006-01-01 평가 신청제한 (등재후보1차)
      2005-01-01 평가 등재후보학술지 유지 (등재후보2차) KCI등재후보
      2004-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2003-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.42 0.42 0.41
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.43 0.43 0.642 0.15
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