메뉴 건너뛰기




Volumn 61, Issue 1, 2005, Pages 16-24

Herbicidal indolizine-5,8-diones: Phostosytem I redox mediators

Author keywords

Chloroplast; Herbicide; Indolizinedione; Photosystem I; Redox mediator; Reduction potential

Indexed keywords

GLUTATHIONE; HERBICIDE; INDOLIZINE 5,8 DIONE; INDOLIZINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 11244292512     PISSN: 1526498X     EISSN: None     Source Type: Journal    
DOI: 10.1002/ps.980     Document Type: Article
Times cited : (54)

References (37)
  • 2
    • 0004058001 scopus 로고    scopus 로고
    • British Crop Protection Council, Farnham, Surrey, UK
    • Tomlin CDS (Ed), The pesticide manual, 12th edn, British Crop Protection Council, Farnham, Surrey, UK (2000).
    • (2000) The Pesticide Manual, 12th Edn
    • Tomlin, C.D.S.1
  • 3
    • 0004058001 scopus 로고    scopus 로고
    • British Crop Protection Council, Farnham, Surrey, UK, version 2.2
    • Tomlin CDS (Ed), The e-pesticide manual, British Crop Protection Council, Farnham, Surrey, UK, version 2.2 (2002-2003).
    • (2002) The E-pesticide Manual
    • Tomlin, C.D.S.1
  • 5
    • 0000317708 scopus 로고
    • Chemistry and biochemistry of PS I herbicides
    • ed by Hutson DH and Roberts TR, Wiley, New York
    • Bowyer JR and Camilleri P, Chemistry and biochemistry of PS I herbicides, in Herbicides, ed by Hutson DH and Roberts TR, Wiley, New York, pp 105-145 (1987).
    • (1987) Herbicides , pp. 105-145
    • Bowyer, J.R.1    Camilleri, P.2
  • 8
    • 0034049079 scopus 로고    scopus 로고
    • Synthesis and characterisation of some 4-keto derivatives of 1,3,4(2H)-isoquinolinetrione redox mediator herbicides
    • Mitchell G, Clarke ED, Ridley SM, Gillen KJ, Vohra SK and Greenhow DT, Synthesis and characterisation of some 4-keto derivatives of 1,3,4(2H)-isoquinolinetrione redox mediator herbicides, Pest Manag Sci 56:127-132 (2000).
    • (2000) Pest Manag Sci , vol.56 , pp. 127-132
    • Mitchell, G.1    Clarke, E.D.2    Ridley, S.M.3    Gillen, K.J.4    Vohra, S.K.5    Greenhow, D.T.6
  • 10
    • 11244292133 scopus 로고    scopus 로고
    • Zeneca, Indolizine-5,8-diones as herbicides, UK Patent 9 219 1410 (1994)
    • Mitchell G, Smith SC and Clarke ED, Zeneca, Indolizine-5,8-diones as herbicides, UK Patent 9 219 1410 (1994).
    • Mitchell, G.1    Smith, S.C.2    Clarke, E.D.3
  • 11
    • 11244292134 scopus 로고    scopus 로고
    • Product class 16: Indolizines
    • Shipman M, Product class 16: indolizines. Science of Synthesis 10:745-787 (2001).
    • (2001) Science of Synthesis , vol.10 , pp. 745-787
    • Shipman, M.1
  • 12
    • 0027048244 scopus 로고
    • Synthesis of indolizine-5,8-diones and [3.2.2]cyclazines
    • Yerxa BR and Moore HW, Synthesis of indolizine-5,8-diones and [3.2.2]cyclazines. Tetrahedron Lett 33:7811-7814 (1992).
    • (1992) Tetrahedron Lett , vol.33 , pp. 7811-7814
    • Yerxa, B.R.1    Moore, H.W.2
  • 13
    • 0001429617 scopus 로고
    • A general, regiospecific synthesis of highly substituted quinones
    • Liebeskind LS, Iyer S and Jewell CF Jr, A general, regiospecific synthesis of highly substituted quinones. J Org Chem 51:3065-3067 (1986).
    • (1986) J Org Chem , vol.51 , pp. 3065-3067
    • Liebeskind, L.S.1    Iyer, S.2    Jewell Jr., C.F.3
  • 14
    • 0345363875 scopus 로고
    • The preparative chemistry of cyclobutenedione: I. Synthesis of cyclobutenedione and alkyl-, alkenyl- and aryl-derivatives
    • Schmidt AH and Reid W, The preparative chemistry of cyclobutenedione: I. Synthesis of cyclobutenedione and alkyl-, alkenyl- and aryl-derivatives. Synthesis 1-22 (1978).
    • (1978) Synthesis , pp. 1-22
    • Schmidt, A.H.1    Reid, W.2
  • 15
    • 84984161555 scopus 로고
    • The preparative chemistry of cyclobutenedione: II. Reactions of alkyl-, alkenyl and arylcyclobutenediones
    • Knorr H and Reid W, The preparative chemistry of cyclobutenedione: II. Reactions of alkyl-, alkenyl and arylcyclobutenediones. Synthesis 649-666 (1978).
    • (1978) Synthesis , pp. 649-666
    • Knorr, H.1    Reid, W.2
  • 16
    • 0018225241 scopus 로고
    • The preparative chemistry of cyclobutenedione: III. Synthesis of squaric acid, benzocyclobutenedione and their derivatives
    • Schmidt AH and Ried W, The preparative chemistry of cyclobutenedione: III. Synthesis of squaric acid, benzocyclobutenedione and their derivatives. Synthesis 869-880 (1978).
    • (1978) Synthesis , pp. 869-880
    • Schmidt, A.H.1    Ried, W.2
  • 18
    • 0000205056 scopus 로고
    • Reactions of squaric acid and some derivatives with thionyl chloride/N,N-dimethylformamide
    • De Selma RC, Fox CJ and Riordan RC, Reactions of squaric acid and some derivatives with thionyl chloride/N,N-dimethylformamide. Tetrahedron Lett 11:781-782 (1970).
    • (1970) Tetrahedron Lett , vol.11 , pp. 781-782
    • De Selma, R.C.1    Fox, C.J.2    Riordan, R.C.3
  • 21
    • 37049088780 scopus 로고
    • Pyrrolo[1,2-b]isoquinoline-5,10-diones and indolizine-5,8-diones
    • Cornforth J and Ming-hui D, Pyrrolo[1,2-b]isoquinoline-5,10-diones and indolizine-5,8-diones. J Chem Soc, Perkin Trans I 1463 (1990).
    • (1990) J Chem Soc, Perkin Trans I , pp. 1463
    • Cornforth, J.1    Ming-hui, D.2
  • 22
    • 77957006380 scopus 로고
    • Preparation of higher plant chloroplasts
    • ed by San Pietro A, Academic Press, London
    • Walker DA, Preparation of higher plant chloroplasts, in Methods in enzymology, ed by San Pietro A, Academic Press, London, Vol 69, pp 94-104 (1980).
    • (1980) Methods in Enzymology , vol.69 , pp. 94-104
    • Walker, D.A.1
  • 24
    • 0004308459 scopus 로고    scopus 로고
    • distributed by Tripos Inc, St Louis, MO, USA
    • CONCORD, Pearlman RS, Concord user's manual, distributed by Tripos Inc, St Louis, MO, USA.
    • Concord User's Manual
    • Pearlman, R.S.1
  • 25
    • 11244255105 scopus 로고
    • AESOP, an in-house molecular mechanics program developed at Zeneca, Inc, Wilmington, DE 19897, USA; derived in part from BIGSTRN-3 (QCPE 514); Nachbar RB Jr and MislowK, QCPE Bull (Quantum Chemistry Program Exchange) 6:96 (1986).
    • (1986) QCPE Bull (Quantum Chemistry Program Exchange) , vol.6 , pp. 96
  • 26
    • 11244262510 scopus 로고    scopus 로고
    • SYBYL, Tripos Inc, 1699 South Hanley Rd, St Louis, Missouri 63 144, USA
    • SYBYL, Tripos Inc, 1699 South Hanley Rd, St Louis, Missouri 63 144, USA (www.tripos.com).
  • 27
    • 11244255551 scopus 로고    scopus 로고
    • Silicon Graphics, Inc, Mountain View, CA 94043, USA
    • Silicon Graphics, Inc, Mountain View, CA 94043, USA (www.sgi.com).
  • 28
    • 0011198787 scopus 로고    scopus 로고
    • with contributions from Amos RD, Buenker RJ, van Dam H, Dupuis M, Handy NC, Hillier IH, Knowles PJ, Bonacic-Koutecky V, von Niessen W, Harrison RJ, Rendell AP, Saunders VR, Schoffel K, Stone AJ and Tozer D
    • GAMESS-UK is a package of ab initio programs written by Guest MF, van Lenthe JH, Kendrick J, and Sherwood P, with contributions from Amos RD, Buenker RJ, van Dam H, Dupuis M, Handy NC, Hillier IH, Knowles PJ, Bonacic-Koutecky V, von Niessen W, Harrison RJ, Rendell AP, Saunders VR, Schoffel K, Stone AJ and Tozer D (http://www.cse.clrc.ac.uk/qcg/gamess-uk/).
    • GAMESS-UK
    • Guest, M.F.1    Van Lenthe, J.H.2    Kendrick, J.3    Sherwood, P.4
  • 29
    • 0000781020 scopus 로고
    • Partial least squares
    • PLS, ed by Kotz S and Johnson NL, J Wiley, New York
    • PLS, Wold H, Partial least squares, in Encyclopedia of the statistical sciences, ed by Kotz S and Johnson NL, J Wiley, New York, pp 581-591 (1985).
    • (1985) Encyclopedia of the Statistical Sciences , pp. 581-591
    • Wold, H.1
  • 30
    • 0031775319 scopus 로고    scopus 로고
    • Metabolism-related assays and their application to agrochemical research: Reactivity of pesticides with glutathione and glutathione transferases
    • Clarke ED, Greenhow DT and Adams D, Metabolism-related assays and their application to agrochemical research: reactivity of pesticides with glutathione and glutathione transferases. Pestic Sci 54:385-393 (1998).
    • (1998) Pestic Sci , vol.54 , pp. 385-393
    • Clarke, E.D.1    Greenhow, D.T.2    Adams, D.3
  • 32
    • 11244309417 scopus 로고    scopus 로고
    • obtained from Advanced Chemistry Development Inc, Toronto, Canada
    • ACD Phys Chem Batch (version 4.76) obtained from Advanced Chemistry Development Inc, Toronto, Canada.
    • ACD Phys Chem Batch (Version 4.76)
  • 33
    • 84872846883 scopus 로고
    • Reduction potentials of one-electron couples involving free radicals in aqueous media
    • Wardman P, Reduction potentials of one-electron couples involving free radicals in aqueous media. J Phys Chem Ref Data 18:1637-1755 (1989).
    • (1989) J Phys Chem Ref Data , vol.18 , pp. 1637-1755
    • Wardman, P.1
  • 34
    • 0000545745 scopus 로고
    • A method for computing one-electron reduction potentials and its application to p-benzoquinone in water at 300K
    • Wheeler RA, A method for computing one-electron reduction potentials and its application to p-benzoquinone in water at 300K. J Am Chem Soc 116:11 048-11 051 (1994).
    • (1994) J Am Chem Soc , vol.116 , pp. 11048-11051
    • Wheeler, R.A.1
  • 35
    • 84932483373 scopus 로고
    • C-Acylation of 5-membered N-heterocycles: I. Acylation at C-2 of imidazoles and benzimidazoles
    • Regel E and Buechel KH, C-Acylation of 5-membered N-heterocycles: I. Acylation at C-2 of imidazoles and benzimidazoles. Justus Liebigs Ann Chem 145-158 (1977).
    • (1977) Justus Liebigs Ann Chem , pp. 145-158
    • Regel, E.1    Buechel, K.H.2
  • 36
    • 2142772911 scopus 로고
    • Effects of substituents in quinonoid compounds
    • Plenum Press, New York
    • Zuman P, Effects of substituents in quinonoid compounds, in Substituent effects in organic polarography, Plenum Press, New York, pp 273-308 (1967).
    • (1967) Substituent Effects in Organic Polarography , pp. 273-308
    • Zuman, P.1
  • 37
    • 0001467602 scopus 로고
    • Ring strain effects III: Reduction and oxidation potential shifts
    • Ricke RD, Rich WE and Ridgway TH, Ring strain effects III: reduction and oxidation potential shifts. J Am Chem Soc 93:1962-1967 (1971).
    • (1971) J Am Chem Soc , vol.93 , pp. 1962-1967
    • Ricke, R.D.1    Rich, W.E.2    Ridgway, T.H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.