메뉴 건너뛰기




Volumn 63, Issue 10, 2007, Pages 974-1001

Aryl chain analogues of the biotin vitamers as potential herbicides. Part 3

Author keywords

Biotin; Biotin vitamers; Enzyme inhibition; Herbicides; Isosters

Indexed keywords

7,8 DIAMINOPELARGONIC ACID; 7,8-DIAMINOPELARGONIC ACID; 7-KETO-8-AMINOPELARGONIC ACID; 8 AMINO 7 OXONONANOIC ACID; AMINO ACID; BIOTIN; DIAMINO ACID; HERBICIDE; UNCLASSIFIED DRUG;

EID: 34548855058     PISSN: 1526498X     EISSN: 15264998     Source Type: Journal    
DOI: 10.1002/ps.1427     Document Type: Article
Times cited : (7)

References (28)
  • 2
    • 0033027170 scopus 로고    scopus 로고
    • The design and synthesis of inhibitors of dethiobiotin synthase as potential herbicides
    • Rendina AR, Taylor WS, Gibson K, Lorimer G, Rayner D, Lockett B, et al., The design and synthesis of inhibitors of dethiobiotin synthase as potential herbicides. Pestic Sci 55:236-247 (1999).
    • (1999) Pestic Sci , vol.55 , pp. 236-247
    • Rendina, A.R.1    Taylor, W.S.2    Gibson, K.3    Lorimer, G.4    Rayner, D.5    Lockett, B.6
  • 5
    • 0031906453 scopus 로고    scopus 로고
    • Acetyl chloride-methanol as a convenient reagent for: A) quantitative formation of amine hydrochlorides; b) carboxylate ester formation; c) mild removal of N-tert-Boc-protective group
    • Nudelman A, Bechor Y, Falb E, Fisher B, Wexler BA and Nudelman A. Acetyl chloride-methanol as a convenient reagent for: a) quantitative formation of amine hydrochlorides; b) carboxylate ester formation; c) mild removal of N-tert-Boc-protective group. Syn Commum 28:471-474 (1998).
    • (1998) Syn Commum , vol.28 , pp. 471-474
    • Nudelman, A.1    Bechor, Y.2    Falb, E.3    Fisher, B.4    Wexler, B.A.5    Nudelman, A.6
  • 6
    • 0001053924 scopus 로고
    • A facile synthesis of primary amines from carboxylic acids by the Curtius rearrangement
    • Todd LC and Poulter CD, A facile synthesis of primary amines from carboxylic acids by the Curtius rearrangement. Tetrahedron Lett 25:3515-3518 (1984).
    • (1984) Tetrahedron Lett , vol.25 , pp. 3515-3518
    • Todd, L.C.1    Poulter, C.D.2
  • 7
    • 0027252082 scopus 로고
    • Synthesis of amphilectane-type diterpenoids: (±)-8-isocyano-10,14-amphilectadiene
    • Piers E and Romero MA, Synthesis of amphilectane-type diterpenoids: (±)-8-isocyano-10,14-amphilectadiene. Tetrahedron 49:791-5800 (1993).
    • (1993) Tetrahedron , vol.49 , pp. 791-5800
    • Piers, E.1    Romero, M.A.2
  • 9
    • 0036986742 scopus 로고    scopus 로고
    • Synthesis and insecticidal activity of 3,5-dimethylbenzoyl moiety modified analogues of N-tert- butyl-N′-(4-ethylbenzoyl)-3,5- dimethylbenzohydrazide
    • Sawada Y, Nakagawa H, Tsukamoto Y, Yanai T, Yokoi S, Yanagi M, et al., Synthesis and insecticidal activity of 3,5-dimethylbenzoyl moiety modified analogues of N-tert- butyl-N′-(4-ethylbenzoyl)-3,5- dimethylbenzohydrazide. Nippon Noyaku Gakkaishi (J Pestic Sci) 27:365-373 (2002).
    • (2002) Nippon Noyaku Gakkaishi (J Pestic Sci) , vol.27 , pp. 365-373
    • Sawada, Y.1    Nakagawa, H.2    Tsukamoto, Y.3    Yanai, T.4    Yokoi, S.5    Yanagi, M.6
  • 10
    • 34548862001 scopus 로고    scopus 로고
    • Szekely I, Kekesi K, Lovasz nee Gaspar M, Botar S, Hadhazy P, Rakoczi I, et al, 2,3,4-Trinor-1,5-inter-m-phenyleneprostacyclin-I2 derivatives and compositions and methods for inhibiting platelet aggregation. US Patent 4,451,483, 29 May 1984
    • Szekely I, Kekesi K, Lovasz nee Gaspar M, Botar S, Hadhazy P, Rakoczi I, et al., 2,3,4-Trinor-1,5-inter-m-phenyleneprostacyclin-I2 derivatives and compositions and methods for inhibiting platelet aggregation. US Patent 4,451,483, 29 May (1984).
  • 11
    • 0033571418 scopus 로고    scopus 로고
    • Unsymmetrical cyclic ureas as HIV-1 protease inhibitors: Novel biaryl indazoles as P2/P2′ substituents
    • Patel M, Rodgers JD, McHugh RJ Jr, Johnson BL, Cordova BC, Klabe RM, et al., Unsymmetrical cyclic ureas as HIV-1 protease inhibitors: novel biaryl indazoles as P2/P2′ substituents. Bioorg Med Chem Lett 9:3217-3220 (1999).
    • (1999) Bioorg Med Chem Lett , vol.9 , pp. 3217-3220
    • Patel, M.1    Rodgers, J.D.2    McHugh Jr, R.J.3    Johnson, B.L.4    Cordova, B.C.5    Klabe, R.M.6
  • 12
    • 0022076992 scopus 로고
    • Phase-transfer-catalyzed methylation of hydroxyaromatic acids, hydroxyaromatic aldehydes, and aromatic polycarboxylic acids
    • Ramaswamy S, Malaiyandi M and Buchanan GW, Phase-transfer-catalyzed methylation of hydroxyaromatic acids, hydroxyaromatic aldehydes, and aromatic polycarboxylic acids. Environ Sci Technol 19:507-512 (1985).
    • (1985) Environ Sci Technol , vol.19 , pp. 507-512
    • Ramaswamy, S.1    Malaiyandi, M.2    Buchanan, G.W.3
  • 14
    • 0025099864 scopus 로고
    • A novel series of selective leukotriene antagonists: Exploration and optimization of the acidic region in 1,6-disubstituted indoles and indazoles
    • Yee YK, Bernstein PR, Adams EJ, Brown FJ, Cronk LA, Hebbel KC, et al., A novel series of selective leukotriene antagonists: exploration and optimization of the acidic region in 1,6-disubstituted indoles and indazoles. J Med Chem 33:2437-2451 (1990).
    • (1990) J Med Chem , vol.33 , pp. 2437-2451
    • Yee, Y.K.1    Bernstein, P.R.2    Adams, E.J.3    Brown, F.J.4    Cronk, L.A.5    Hebbel, K.C.6
  • 15
    • 0001575724 scopus 로고
    • The synthesis and selected chemistry of 6-alkyl-6-carbalkoxy- and 6-alkyl-6-(aminocarbonyl)-2,4-cyclohexadien-1-ones and cyclohexadienone ketals
    • Schultz AG, Dittami JP, Lavieri FP, Salowey C, Sundararaman P and Szymula MB, The synthesis and selected chemistry of 6-alkyl-6-carbalkoxy- and 6-alkyl-6-(aminocarbonyl)-2,4-cyclohexadien-1-ones and cyclohexadienone ketals. J Org Chem 49:4429-4440 (1984).
    • (1984) J Org Chem , vol.49 , pp. 4429-4440
    • Schultz, A.G.1    Dittami, J.P.2    Lavieri, F.P.3    Salowey, C.4    Sundararaman, P.5    Szymula, M.B.6
  • 16
    • 0008514114 scopus 로고
    • Intramolecular 2 + 2 photocycloadditions of 4-(3′-alkenyl)-and 4-(3′-pentynyl)-2,5- cyclohexadien-1-ones
    • Schultz AG, Plummer M, Taveras AG and Kullnig RK, Intramolecular 2 + 2 photocycloadditions of 4-(3′-alkenyl)-and 4-(3′-pentynyl)-2,5- cyclohexadien-1-ones. J Am Chem Soc 110:5547-5555 (1988).
    • (1988) J Am Chem Soc , vol.110 , pp. 5547-5555
    • Schultz, A.G.1    Plummer, M.2    Taveras, A.G.3    Kullnig, R.K.4
  • 17
    • 0029790092 scopus 로고    scopus 로고
    • Isophthalate-terminated dendrimers: Versatile nanoscopic building blocks with readily modifiable surface functionalities
    • Leon WJ, Kawa M and Frechet JMJ, Isophthalate-terminated dendrimers: versatile nanoscopic building blocks with readily modifiable surface functionalities. J Am Chem Soc 118:8847-8859 (1996).
    • (1996) J Am Chem Soc , vol.118 , pp. 8847-8859
    • Leon, W.J.1    Kawa, M.2    Frechet, J.M.J.3
  • 18
    • 0008640101 scopus 로고
    • Alkylation of a-formamido ketone enolate anions. A versatile synthesis of a-alkyl a-amino ketones
    • Ackrell J, Muchowski JM, Galeazzi E and Guzman A, Alkylation of a-formamido ketone enolate anions. A versatile synthesis of a-alkyl a-amino ketones. J Org Chem 51:3374-3376 (1986).
    • (1986) J Org Chem , vol.51 , pp. 3374-3376
    • Ackrell, J.1    Muchowski, J.M.2    Galeazzi, E.3    Guzman, A.4
  • 19
    • 0037038325 scopus 로고    scopus 로고
    • Identification of potent and selective small-molecule inhibitors of caspase-3 through the use of extended tethering and structure-based drug design
    • Choong IC, Lew W, Lee D, Pham P, Burdett MT, Lam JW, et al., Identification of potent and selective small-molecule inhibitors of caspase-3 through the use of extended tethering and structure-based drug design. J Med Chem 45:5005-5022 (2002).
    • (2002) J Med Chem , vol.45 , pp. 5005-5022
    • Choong, I.C.1    Lew, W.2    Lee, D.3    Pham, P.4    Burdett, M.T.5    Lam, J.W.6
  • 20
    • 34548842170 scopus 로고    scopus 로고
    • Sircar JC and Capitis T, 4-Hydroxy-N-[5, substituted hetero) methyl]-3-isoxazolyl]-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide and 4-hydroxy-2-alkyl-N-[5, substituted hetero)methyl]-3-isoxazolyl]-2H- 1,2-benzothiazine-3-carboxamide 1,1-dioxide. European Patent Application 1984
    • Sircar JC and Capitis T, 4-Hydroxy-N-[5-[(substituted hetero) methyl]-3-isoxazolyl]-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide and 4-hydroxy-2-alkyl-N-[5-[(substituted hetero)methyl]-3-isoxazolyl]-2H- 1,2-benzothiazine-3-carboxamide 1,1-dioxide. European Patent Application (1984).
  • 21
    • 0001173379 scopus 로고
    • Oxidation of 2,4-alkadienoic esters with selenium dioxide. A new synthesis of furans and selenophenes
    • Tsuboi S, Mimura S, Ono S, Watanabe K and Takeda A, Oxidation of 2,4-alkadienoic esters with selenium dioxide. A new synthesis of furans and selenophenes. Bull Soc Chim Jpn 60:1807-1812 (1987).
    • (1987) Bull Soc Chim Jpn , vol.60 , pp. 1807-1812
    • Tsuboi, S.1    Mimura, S.2    Ono, S.3    Watanabe, K.4    Takeda, A.5
  • 22
    • 0001404878 scopus 로고
    • A convenient method for the preparation of 1-(tert-butyloxycarbonyl)pyrroles
    • Grehn L and Ragnarsson U, A convenient method for the preparation of 1-(tert-butyloxycarbonyl)pyrroles. Angew Chem 96:291-292 (1984).
    • (1984) Angew Chem , vol.96 , pp. 291-292
    • Grehn, L.1    Ragnarsson, U.2
  • 23
    • 0026707660 scopus 로고
    • Generation and use of a zinc derivative of a functionalized 1,3-oxazole. Solution of the virginiamycin/ madumycin oxazole problem
    • Gangloff AR, Aakermark B and Helquist P, Generation and use of a zinc derivative of a functionalized 1,3-oxazole. Solution of the virginiamycin/ madumycin oxazole problem. J Org Chem 57:4797-4799 (1992).
    • (1992) J Org Chem , vol.57 , pp. 4797-4799
    • Gangloff, A.R.1    Aakermark, B.2    Helquist, P.3
  • 25
    • 0001506363 scopus 로고
    • The use of cysteine- and serine-derived thiazolidinethiones and oxazolidinethione as efficient chiral auxiliaries in aldol condensations
    • Hsiao C, Liu L and Miller MJ, The use of cysteine- and serine-derived thiazolidinethiones and oxazolidinethione as efficient chiral auxiliaries in aldol condensations. J Org Chem 52:2201-2206 (1987).
    • (1987) J Org Chem , vol.52 , pp. 2201-2206
    • Hsiao, C.1    Liu, L.2    Miller, M.J.3
  • 26
    • 0002000355 scopus 로고
    • Isolation of photorespiration mutants in Arabidopsis thaliana
    • ed. by Edelman M, Hallick RB and Chua NH. Elsevier Biomedical Press, Amsterdam, pp
    • Somerville CR and Ogren WL, Isolation of photorespiration mutants in Arabidopsis thaliana, in Methods in Chloroplast Molecular Biology, ed. by Edelman M, Hallick RB and Chua NH. Elsevier Biomedical Press, Amsterdam, pp. 129-138 (1982).
    • (1982) Methods in Chloroplast Molecular Biology , pp. 129-138
    • Somerville, C.R.1    Ogren, W.L.2
  • 27
    • 0025827163 scopus 로고
    • Asymmetric synthesis. Practical production of D and L threonine. Dynamic kinetic resolution in rhodium and ruthenium catalyzed hydrogenation of 2-(acylamino)-3-oxobutyrates
    • Genet JP, Pinel C, Mallart S, Juge S, Thorimbert S and Laffitte JA, Asymmetric synthesis. Practical production of D and L threonine. Dynamic kinetic resolution in rhodium and ruthenium catalyzed hydrogenation of 2-(acylamino)-3-oxobutyrates. Tetrahedron Asymm 2:555-567 (1991).
    • (1991) Tetrahedron Asymm , vol.2 , pp. 555-567
    • Genet, J.P.1    Pinel, C.2    Mallart, S.3    Juge, S.4    Thorimbert, S.5    Laffitte, J.A.6
  • 28


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.