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Volumn 56, Issue 20, 2008, Pages 9434-9440

Synthesis and phytotoxic activity of ozonides

Author keywords

4 + 3 cycloaddition; Herbicides; Oxabicycles; Oxallyl cation; Ozonides; Plant growth regulators

Indexed keywords

1,2,4 TRIOXANE; 1,2,4-TRIOXANE; HERBICIDE; HETEROCYCLIC COMPOUND;

EID: 55549116728     PISSN: 00218561     EISSN: None     Source Type: Journal    
DOI: 10.1021/jf802077e     Document Type: Article
Times cited : (22)

References (31)
  • 1
    • 0021948029 scopus 로고
    • (Artemisinin): An antimalarial drug from China
    • Klayman, D. L. Qinghaosu (Artemisinin): an antimalarial drug from China. Science 1985, 228, 1049-1055.
    • (1985) Science , vol.228 , pp. 1049-1055
    • Klayman, D.L.Q.1
  • 3
    • 0035207181 scopus 로고    scopus 로고
    • Why artemisinin and certain synthetic peroxides are potent antimalarials. Implications for the mode of action
    • Jefford, C. W. Why artemisinin and certain synthetic peroxides are potent antimalarials. Implications for the mode of action. Curr. Med. Chem. 2001, 8, 1803-1826.
    • (2001) Curr. Med. Chem , vol.8 , pp. 1803-1826
    • Jefford, C.W.1
  • 4
    • 4344662233 scopus 로고    scopus 로고
    • A worthy adversary for malaria
    • O'Neil, P. M. A worthy adversary for malaria. Nature 2004, 430, 838-839.
    • (2004) Nature , vol.430 , pp. 838-839
    • O'Neil, P.M.1
  • 6
    • 0000799076 scopus 로고
    • Artemisinin, a constituent of annual wormwood (Artemisia annua), is a selective phytotoxin
    • Duke, S. O.; Vaughn, K. C.; Croom, E. M., Jr.; Elsohly, H. N. Artemisinin, a constituent of annual wormwood (Artemisia annua), is a selective phytotoxin. Weed Sci. 1987, 35, 499-505.
    • (1987) Weed Sci , vol.35 , pp. 499-505
    • Duke, S.O.1    Vaughn, K.C.2    Croom Jr., E.M.3    Elsohly, H.N.4
  • 7
    • 0041358479 scopus 로고    scopus 로고
    • The phytotoxic effects of artemisinin and related compounds of Artemisia annua
    • Bagchi, G. D.; Jain, D. C.; Kumar, S. The phytotoxic effects of artemisinin and related compounds of Artemisia annua. J. Med. Arom. Plant Sci. 1998, 20, 5-11.
    • (1998) J. Med. Arom. Plant Sci , vol.20 , pp. 5-11
    • Bagchi, G.D.1    Jain, D.C.2    Kumar, S.3
  • 8
    • 0001616158 scopus 로고
    • Plant growth regulatory activities of artemisinin and its related compounds
    • Chen, P. K.; Leather, G. R. Plant growth regulatory activities of artemisinin and its related compounds. J. Chem. Ecol. 1990, 16, 1867-1876.
    • (1990) J. Chem. Ecol , vol.16 , pp. 1867-1876
    • Chen, P.K.1    Leather, G.R.2
  • 11
    • 37049111573 scopus 로고
    • Isolation and characterization of a stable ozonide during an attempted synthesis of structural analogues of sarkomycin
    • Cummins, W. J.; Drew, M. G. B.; Mann, J.; Walsh, E. B. Isolation and characterization of a stable ozonide during an attempted synthesis of structural analogues of sarkomycin. J. Chem. Soc. Perkin Trans. 1 1983, 167-171.
    • (1983) J. Chem. Soc. Perkin Trans. 1 , pp. 167-171
    • Cummins, W.J.1    Drew, M.G.B.2    Mann, J.3    Walsh, E.B.4
  • 15
    • 33750945847 scopus 로고    scopus 로고
    • New helminthosporal analogues with plant-growth regulatory properties synthesized via oxyallyl cation
    • Chaves, F. C.; Barbosa, L. C. A.; Demuner, A. J.; Silva, A. A. New helminthosporal analogues with plant-growth regulatory properties synthesized via oxyallyl cation. Z. Naturforsch. 2006, 61b, 1287-1294.
    • (2006) Z. Naturforsch , vol.61 b , pp. 1287-1294
    • Chaves, F.C.1    Barbosa, L.C.A.2    Demuner, A.J.3    Silva, A.A.4
  • 16
    • 11244258624 scopus 로고    scopus 로고
    • Barbosa, L. C. A.; Costa, A. V.; Veloso, D. P.; Lopes, J. L. C.; Terrones, M.; G, H.; Diaz, B. K.; Hennsen, B. L. Phytogrowth-inhibitory lactones derivatives of Glaucolide B. Z. Naturforsch. 2004, 59c, 803-810.
    • Barbosa, L. C. A.; Costa, A. V.; Veloso, D. P.; Lopes, J. L. C.; Terrones, M.; G, H.; Diaz, B. K.; Hennsen, B. L. Phytogrowth-inhibitory lactones derivatives of Glaucolide B. Z. Naturforsch. 2004, 59c, 803-810.
  • 18
    • 35548938583 scopus 로고    scopus 로고
    • Synthesis of 3-(4-bromobenzyl)-5-(arylmethylene)-5H-furan-2-ones and their activity as inhibitors of the photosynthetic electron transport chain
    • Barbosa, L. C. A.; Rocha, M. E.; Teixeira, R. R.; Maltha, C. R. A.; Forlani, G. Synthesis of 3-(4-bromobenzyl)-5-(arylmethylene)-5H-furan-2-ones and their activity as inhibitors of the photosynthetic electron transport chain. J. Agric. Food Chem. 2007, 55, 8562-8569.
    • (2007) J. Agric. Food Chem , vol.55 , pp. 8562-8569
    • Barbosa, L.C.A.1    Rocha, M.E.2    Teixeira, R.R.3    Maltha, C.R.A.4    Forlani, G.5
  • 19
    • 42449113019 scopus 로고    scopus 로고
    • Teixeira, R. R.; Barbosa, L. C. A.; Forlani, G.; Pilo-Veloso, D.; Carneiro, J. W. de M. Synthesis of photosynthesis-inhibiting nostoclide analogues. J. Agric. Food Chem. 2008, 56, 2321-2329.
    • Teixeira, R. R.; Barbosa, L. C. A.; Forlani, G.; Pilo-Veloso, D.; Carneiro, J. W. de M. Synthesis of photosynthesis-inhibiting nostoclide analogues. J. Agric. Food Chem. 2008, 56, 2321-2329.
  • 20
    • 0033230116 scopus 로고    scopus 로고
    • Costa, A. V.; Barbosa, L. C. A.; Demuner, A. J.; Silva, A. A. Synthesis and herbicidal activity of 2α,4α-dimethyl-8-oxabicyclo[3.2.1]oct-6- en-3-one derivatives. J. Agric. Food Chem. 1999, 47, 4807-4814.
    • Costa, A. V.; Barbosa, L. C. A.; Demuner, A. J.; Silva, A. A. Synthesis and herbicidal activity of 2α,4α-dimethyl-8-oxabicyclo[3.2.1]oct-6- en-3-one derivatives. J. Agric. Food Chem. 1999, 47, 4807-4814.
  • 21
    • 0141719465 scopus 로고    scopus 로고
    • Demuner, A. J.; Barbosa, L. C. A.; Piló-Veloso, D. New 8-oxabicyclo[3.2.1]oct-6-en-3-one derivatives with plant growth regulatory activity. J. Agric. Food Chem. 1998, 46, 1173-1176.
    • Demuner, A. J.; Barbosa, L. C. A.; Piló-Veloso, D. New 8-oxabicyclo[3.2.1]oct-6-en-3-one derivatives with plant growth regulatory activity. J. Agric. Food Chem. 1998, 46, 1173-1176.
  • 23
    • 0000110756 scopus 로고
    • Steric effects, as well σ*-orbital energies, are important in diastereoface differentiation in additions to chiral aldehydes
    • Lodge, E. P.; Heathcock, C. H. Steric effects, as well σ*-orbital energies, are important in diastereoface differentiation in additions to chiral aldehydes. J. Am. Chem. Soc. 1987, 109, 3353-3361.
    • (1987) J. Am. Chem. Soc , vol.109 , pp. 3353-3361
    • Lodge, E.P.1    Heathcock, C.H.2
  • 24
    • 20444391160 scopus 로고    scopus 로고
    • Barbosa, L. C. A.; Maltha, C. R. A.; Demuner, A. J.; Filomeno, C. A.; Silva, A. A. Síntese de novos herbicidas derivados do 1,2α,4α,5-tetrametil-8-oxabiciclo[3.2.1]oct-6-en-3-ona. Quim. Nova 2004, 27, 241-246.
    • Barbosa, L. C. A.; Maltha, C. R. A.; Demuner, A. J.; Filomeno, C. A.; Silva, A. A. Síntese de novos herbicidas derivados do 1,2α,4α,5-tetrametil-8-oxabiciclo[3.2.1]oct-6-en-3-ona. Quim. Nova 2004, 27, 241-246.
  • 25
    • 0011178547 scopus 로고
    • Synergistic effects of four cinnamic acid compounds on grain sorghum
    • Einhellig, F. A.; Schon, M. K.; Rasmussen, J. A. Synergistic effects of four cinnamic acid compounds on grain sorghum. Plant Growth Regul. 1983, 1, 251-258.
    • (1983) Plant Growth Regul , vol.1 , pp. 251-258
    • Einhellig, F.A.1    Schon, M.K.2    Rasmussen, J.A.3
  • 27
    • 0002320788 scopus 로고    scopus 로고
    • 3 + 4] Cycloadditions via oxyallyl cátions: Applications in organic synthesis
    • Demuner, A. J.; Barbosa, L. C. A.; Piló-Veloso, D. [3 + 4] Cycloadditions via oxyallyl cátions: applications in organic synthesis. Quim. Nova 1997, 20, 18-29.
    • (1997) Quim. Nova , vol.20 , pp. 18-29
    • Demuner, A.J.1    Barbosa, L.C.A.2    Piló-Veloso, D.3
  • 29
    • 0001317795 scopus 로고
    • Potential allelopathic activity of several sesquiterpene lactone models
    • Macías, F. A.; Galindo, J. C. G.; Massanet, G. M. Potential allelopathic activity of several sesquiterpene lactone models. Phytochemistry 1992, 31, 1969-1977.
    • (1992) Phytochemistry , vol.31 , pp. 1969-1977
    • Macías, F.A.1    Galindo, J.C.G.2    Massanet, G.M.3
  • 30
    • 0041986859 scopus 로고    scopus 로고
    • The use of diethylzinc for the generation of oxyallyl cations from polybromo ketones and their reactions with substituted furans
    • Barbosa, L. C. A.; Mann, J. The use of diethylzinc for the generation of oxyallyl cations from polybromo ketones and their reactions with substituted furans. Synthesis 1996, 1, 31-33.
    • (1996) Synthesis , vol.1 , pp. 31-33
    • Barbosa, L.C.A.1    Mann, J.2
  • 31
    • 0000036757 scopus 로고
    • Trost, B. M, Fleming, I, Eds, Pergamon Press: Oxford
    • Lee, D. G.; Chen, T. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford, 1991; Vol. 7, pp 541-591.
    • (1991) Comprehensive Organic Synthesis , vol.7 , pp. 541-591
    • Lee, D.G.1    Chen, T.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.