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Volumn 24, Issue 3, 2005, Pages 275-296

Bioactive pseudo-C-nucleosides containing thiazole, thiazolidinone, and tetrazole rings

Author keywords

Alzheimer disease; DFT calculations; Insecticidal activity; Neuroactivity; Pseudo C nucleosides; Synthesis

Indexed keywords

HEXAPODA; INSECTA; MUSCA DOMESTICA;

EID: 27944492386     PISSN: 07328303     EISSN: 15322327     Source Type: Journal    
DOI: 10.1081/CAR-200060396     Document Type: Article
Times cited : (29)

References (65)
  • 3
    • 0021990687 scopus 로고
    • Relationships between the cytotoxicity of tiazofurin and its metabolism by cultured human-lung cancer-cells
    • Carney, D.N.; Ahluwalia, G.S.; Jayaram, H.N.; Cooney, D.A.; Johns, D.G. Relationships between the cytotoxicity of tiazofurin and its metabolism by cultured human-lung cancer-cells. J. Clin. Invest. 1985, 75 (1), 175-182.
    • (1985) J. Clin. Invest. , vol.75 , Issue.1 , pp. 175-182
    • Carney, D.N.1    Ahluwalia, G.S.2    Jayaram, H.N.3    Cooney, D.A.4    Johns, D.G.5
  • 4
    • 0030848893 scopus 로고    scopus 로고
    • Synthesis of nonhydrolyzable analogues of thiazole-4-carboxamide and benzamide adenine dinucleotide containing fluorine atom at the C2′ of adenine nucleoside: Induction of K562 differentiation and inosine monophosphate dehydrogenase inhibitory activity
    • Lesiak, K.; Watanabe, K.A.; Majumdar, A.; Seidman, M.; Vanderveen, K.; Goldstein, B.M.; Pankiewicz, K.W. Synthesis of nonhydrolyzable analogues of thiazole-4-carboxamide and benzamide adenine dinucleotide containing fluorine atom at the C2′ of adenine nucleoside: induction of K562 differentiation and inosine monophosphate dehydrogenase inhibitory activity. J. Med. Chem. 1997, 40, 2533-2538.
    • (1997) J. Med. Chem. , vol.40 , pp. 2533-2538
    • Lesiak, K.1    Watanabe, K.A.2    Majumdar, A.3    Seidman, M.4    Vanderveen, K.5    Goldstein, B.M.6    Pankiewicz, K.W.7
  • 5
    • 0036566861 scopus 로고    scopus 로고
    • A synthesis of a hydroxyvaline-derived thiazole-4-carboxylate constituting an antibiotic, thiocilline I
    • Yonezawa, Y.; Saito, H.; Suzuki, S.; Shin, C. A synthesis of a hydroxyvaline-derived thiazole-4-carboxylate constituting an antibiotic, thiocilline I. Heterocycles 2002, 57 (5), 903-908.
    • (2002) Heterocycles , vol.57 , Issue.5 , pp. 903-908
    • Yonezawa, Y.1    Saito, H.2    Suzuki, S.3    Shin, C.4
  • 6
    • 0031439957 scopus 로고    scopus 로고
    • Oxidative DNA cleavage by the antitumor antibiotic leinamycin and simple 1,2-dithiolan-3-one 1-oxides: Evidence for thiol-dependent conversion of molecular oxygen to DNA-cleaving oxygen radicals mediated by polysulfides
    • Mitra, K.; Kim, W.; Daniels, J.S.; Gates, K.S. Oxidative DNA cleavage by the antitumor antibiotic leinamycin and simple 1,2-dithiolan-3-one 1-oxides: evidence for thiol-dependent conversion of molecular oxygen to DNA-cleaving oxygen radicals mediated by polysulfides. J. Am. Chem. Soc. 1997, 119, 11691-11692.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 11691-11692
    • Mitra, K.1    Kim, W.2    Daniels, J.S.3    Gates, K.S.4
  • 8
    • 0030841236 scopus 로고    scopus 로고
    • Marine natural products
    • Faulkner, D.J. Marine natural products. Nat. Prod. Rep. 1997, 14 (3), 259-302.
    • (1997) Nat. Prod. Rep. , vol.14 , Issue.3 , pp. 259-302
    • Faulkner, D.J.1
  • 9
    • 0023792179 scopus 로고
    • Patellazole-C - A potent cytotoxic macrolide from Lissoclinum patella
    • Zabriskie, T.M.; Mayne, C.L.; Ireland, C.M. Patellazole-C - a potent cytotoxic macrolide from Lissoclinum patella. J. Am. Chem. Soc. 1988, 110 (23), 7919-7920.
    • (1988) J. Am. Chem. Soc. , vol.110 , Issue.23 , pp. 7919-7920
    • Zabriskie, T.M.1    Mayne, C.L.2    Ireland, C.M.3
  • 10
    • 0026044572 scopus 로고
    • Pateamine - A potent cytotoxin from the New-Zealand marine sponge, Mycale sp.
    • Northcote, P.; Blunt, J.; Munro, M. Pateamine - a potent cytotoxin from the New-Zealand marine sponge, Mycale sp. Tetrahedron Lett. 1991, 32 (44), 6411-6414.
    • (1991) Tetrahedron Lett. , vol.32 , Issue.44 , pp. 6411-6414
    • Northcote, P.1    Blunt, J.2    Munro, M.3
  • 11
    • 0028258027 scopus 로고
    • Structure of curacin-A, a novel antimitotic, antiproliferative, and brine shrimp toxic natural product from the marine Cyanobacterium lyngbya-majuscula
    • Gerwick, W.H.; Proteau, P.J.; Nagle, D.G.; Hamet, E.; Blokkin, A.; State, D. Structure of curacin-A, a novel antimitotic, antiproliferative, and brine shrimp toxic natural product from the marine Cyanobacterium lyngbya-majuscula.. J. Org. Chem. 1994, 59 (6), 1243-1245.
    • (1994) J. Org. Chem. , vol.59 , Issue.6 , pp. 1243-1245
    • Gerwick, W.H.1    Proteau, P.J.2    Nagle, D.G.3    Hamet, E.4    Blokkin, A.5    State, D.6
  • 12
    • 0023926362 scopus 로고
    • Mycothiazole, a polyketide heterocycle from a marine sponge
    • Crews, P.; Kakou, Y.; Quiñoa, E. Mycothiazole, a polyketide heterocycle from a marine sponge. J. Am. Chem. Soc. 1988, 110 (13), 4365-4368.
    • (1988) J. Am. Chem. Soc. , vol.110 , Issue.13 , pp. 4365-4368
    • Crews, P.1    Kakou, Y.2    Quiñoa, E.3
  • 14
    • 57249083896 scopus 로고    scopus 로고
    • New 6-(4-bromophenyl)imidazo[2,1-b]thiazole derivatives: Synthesis and antimicrobial activity
    • Ulusoy, N.; Kiraz, M.; Kucukbasmaci, O. New 6-(4-bromophenyl)imidazo[2,1- b]thiazole derivatives: synthesis and antimicrobial activity. Monatsh. Chem. 2002, 133 (10), 1305-1315.
    • (2002) Monatsh. Chem. , vol.133 , Issue.10 , pp. 1305-1315
    • Ulusoy, N.1    Kiraz, M.2    Kucukbasmaci, O.3
  • 15
    • 0035814035 scopus 로고    scopus 로고
    • Synthesis and anti-inflammatory, analgesic activity of 3,3′-(1,2-ethanediyl)-bis[2-aryl-4-thiazolidinone] chiral compounds. Part 10
    • Vigorita, M.G.; Ottanà, R.; Monforte, F.; Maccari, R.; Trovato, A.; Monforte, M.T.; Taviano, M.F. Synthesis and anti-inflammatory, analgesic activity of 3,3′-(1,2-ethanediyl)-bis[2-aryl-4-thiazolidinone] chiral compounds. Part 10. Bioorg. Med. Chem. Lett. 2001, 11, 2791-2794.
    • (2001) Bioorg. Med. Chem. Lett. , vol.11 , pp. 2791-2794
    • Vigorita, M.G.1    Ottanà, R.2    Monforte, F.3    Maccari, R.4    Trovato, A.5    Monforte, M.T.6    Taviano, M.F.7
  • 16
    • 0034878692 scopus 로고    scopus 로고
    • Theoretical elucidation of structure-antioxidant activity relationships for thiazolidinone derivatives
    • Sun, Y.-M.; Wang, X.-L.; Zhang, H.-Y.; Chen, D.-Z. Theoretical elucidation of structure-antioxidant activity relationships for thiazolidinone derivatives. Quant. Struct.-Act. Relat. 2001, 20, 139-142.
    • (2001) Quant. Struct.-Act. Relat. , vol.20 , pp. 139-142
    • Sun, Y.-M.1    Wang, X.-L.2    Zhang, H.-Y.3    Chen, D.-Z.4
  • 17
    • 0036806068 scopus 로고    scopus 로고
    • Synthesis and primary cytotoxicity evaluation of new 5-bromo-3- substituted-hydrazono-1H-2-indolinones
    • Karali, N.; Terzioǧlu, N.; Gürsoy, A. Synthesis and primary cytotoxicity evaluation of new 5-bromo-3-substituted-hydrazono-1H-2-indolinones. Arch. Pharm. Pharm. Med. Chem. 2002, 8, 374-380.
    • (2002) Arch. Pharm. Pharm. Med. Chem. , vol.8 , pp. 374-380
    • Karali, N.1    Terzioǧlu, N.2    Gürsoy, A.3
  • 19
    • 0034350337 scopus 로고    scopus 로고
    • Synthesis, characterisation and applications of some new 5-substituted-4-thiazolidinone-2-thioxo azo derivatives
    • Bajpai, R.; Tiwari, S.; Tiwari, K.S.; Tiwari, B.M.L. Synthesis, characterisation and applications of some new 5-substituted-4-thiazolidinone-2- thioxo azo derivatives. Asian J. Chem. 2000, 12 (4), 1199-1208.
    • (2000) Asian J. Chem. , vol.12 , Issue.4 , pp. 1199-1208
    • Bajpai, R.1    Tiwari, S.2    Tiwari, K.S.3    Tiwari, B.M.L.4
  • 20
    • 0037212742 scopus 로고    scopus 로고
    • Synthesis and antifungal and insecticidal activity studies of 2-(aryl/furyl)-5-H-4-thiazolidinone sulphadiazines
    • Jain, V.K.; Rao, J.T. Synthesis and antifungal and insecticidal activity studies of 2-(aryl/furyl)-5-H-4-thiazolidinone sulphadiazines. Asian J. Chem. 2003, 15 (1), 483-486.
    • (2003) Asian J. Chem. , vol.15 , Issue.1 , pp. 483-486
    • Jain, V.K.1    Rao, J.T.2
  • 21
    • 0025069980 scopus 로고
    • 1,2,4-diazaphosphole nucleosides - Synthesis, structure, and antitumor activity of nucleosides with a lambda-3 phosphorus atom
    • Riley, T.A.; Larson, S.B.; Avery, T.L.; Finch, R.A.; Robins, R.K. 1,2,4-diazaphosphole nucleosides - synthesis, structure, and antitumor activity of nucleosides with a lambda-3 phosphorus atom. J. Med. Chem. 1990, 33 (2), 572-576.
    • (1990) J. Med. Chem. , vol.33 , Issue.2 , pp. 572-576
    • Riley, T.A.1    Larson, S.B.2    Avery, T.L.3    Finch, R.A.4    Robins, R.K.5
  • 24
    • 0035835009 scopus 로고    scopus 로고
    • Acid-catalyzed dehydrative cyclization of 4-(D-galacto-pentitol-1-yl)-2- phenyl-2H-1,2,3-triazole. Synthesis and anomeric configuration of D-lyxo-C-nucleoside analogs
    • Sallam, M.A.E.; Megid, S.M.E.A.; Townsend, L.B. Acid-catalyzed dehydrative cyclization of 4-(D-galacto-pentitol-1-yl)-2-phenyl-2H-1,2,3- triazole. Synthesis and anomeric configuration of D-lyxo-C-nucleoside analogs. Carbohydr. Res. 2001, 330, 53-63.
    • (2001) Carbohydr. Res. , vol.330 , pp. 53-63
    • Sallam, M.A.E.1    Megid, S.M.E.A.2    Townsend, L.B.3
  • 25
    • 0035059411 scopus 로고    scopus 로고
    • Synthesis of modified oligonucleotides containing 4-guanidino-2- pyrimidinone nucleobases
    • Robles, J.; Grandas, A.; Pedroso, E. Synthesis of modified oligonucleotides containing 4-guanidino-2-pyrimidinone nucleobases. Tetrahedron 2001, 57, 179-194.
    • (2001) Tetrahedron , vol.57 , pp. 179-194
    • Robles, J.1    Grandas, A.2    Pedroso, E.3
  • 26
    • 2442616178 scopus 로고    scopus 로고
    • Synthesis, bleaching activity, and germination promoting activity of 3,4-disubstituted-4H-1,2,4-triazoles
    • Yamada, N.; Kusano, D.; Kuwano, E. Synthesis, bleaching activity, and germination promoting activity of 3,4-disubstituted-4H-1,2,4-triazoles. J. Fac. Agr. Kyushu U. 2002, 47(1), 67-76.
    • (2002) J. Fac. Agr. Kyushu U. , vol.47 , Issue.1 , pp. 67-76
    • Yamada, N.1    Kusano, D.2    Kuwano, E.3
  • 27
    • 0038289192 scopus 로고    scopus 로고
    • Synthesis of some 1-(2,4-dihydroxythiobenzoyl)imidazoles, -imidazolines and -tetrazoles and their potent activity against Candida species
    • Matysiak, J.; Niewiadomy, A.; Krajewska-Kulak, E.; Macik-Niewiadomy, G. Synthesis of some 1-(2,4-dihydroxythiobenzoyl)imidazoles, -imidazolines and -tetrazoles and their potent activity against Candida species. Farmaco 2003, 58 (6), 455-461.
    • (2003) Farmaco , vol.58 , Issue.6 , pp. 455-461
    • Matysiak, J.1    Niewiadomy, A.2    Krajewska-Kulak, E.3    Macik-Niewiadomy, G.4
  • 28
    • 0542395829 scopus 로고    scopus 로고
    • Microwave assisted synthesis and antifungal activity of 1,2,4-triazine, 1,2,4-triazole, tetrazole and pyrazole derivatives
    • Kidwai, M.; Goel, Y.; Kumar, R. Microwave assisted synthesis and antifungal activity of 1,2,4-triazine, 1,2,4-triazole, tetrazole and pyrazole derivatives. Indian J. Chem. Section B, Organic including Medicinal 1998, 37 (2), 174-179.
    • (1998) Indian J. Chem. Section B, Organic Including Medicinal , vol.37 , Issue.2 , pp. 174-179
    • Kidwai, M.1    Goel, Y.2    Kumar, R.3
  • 29
    • 0024498453 scopus 로고
    • Synthesis and pesticidal activity of some quinazolin-4(3H)-one derivatives
    • Gupta, A.K.S.; Pandey, A.K. Synthesis and pesticidal activity of some quinazolin-4(3H)-one derivatives. Pesticide Sci. 1989, 26 (1), 41-49.
    • (1989) Pesticide Sci. , vol.26 , Issue.1 , pp. 41-49
    • Gupta, A.K.S.1    Pandey, A.K.2
  • 30
    • 0034553416 scopus 로고    scopus 로고
    • Synthesis and properties of aminoacylamido-AMP: Chemical optimization for the construction of an N-acyl phosphoramidate linkage
    • Moriguchi, T.; Yanagi, T.; Kunimori, M.; Wada, T.; Sekine, M. Synthesis and properties of aminoacylamido-AMP: chemical optimization for the construction of an N-acyl phosphoramidate linkage. J. Org. Chem. 2000, 65, 8229-8238.
    • (2000) J. Org. Chem. , vol.65 , pp. 8229-8238
    • Moriguchi, T.1    Yanagi, T.2    Kunimori, M.3    Wada, T.4    Sekine, M.5
  • 31
    • 0001517609 scopus 로고    scopus 로고
    • Mechanism of action of cholinesterase inhibitors
    • Giacobini, E., Dunitz, M., Eds.; Genève
    • Rainer, E.; Radic, Z. Mechanism of action of cholinesterase inhibitors. In Cholinesterases and Cholinesterase Inhibitors; Giacobini, E., Dunitz, M., Eds.; Genève, 2000; 103-118.
    • (2000) Cholinesterases and Cholinesterase Inhibitors , pp. 103-118
    • Rainer, E.1    Radic, Z.2
  • 33
    • 0033774824 scopus 로고    scopus 로고
    • Tetrabutylammonium peroxydisulfate in organic synthesis X. An efficient nickel-catalysed one-pot synthesis of nitriles from aldehydes by oxidation with tetrabutylammonium peroxydisulfate
    • Chen, F.-E.; Fu, H.; Meng, G.; Cheng, Y.; Lü, Y.-X. Tetrabutylammonium peroxydisulfate in organic synthesis X. An efficient nickel-catalysed one-pot synthesis of nitriles from aldehydes by oxidation with tetrabutylammonium peroxydisulfate. Synthesis 2000, 11, 1519-1520.
    • (2000) Synthesis , vol.11 , pp. 1519-1520
    • Chen, F.-E.1    Fu, H.2    Meng, G.3    Cheng, Y.4    Lü, Y.-X.5
  • 34
    • 0035152573 scopus 로고    scopus 로고
    • A simple and highly efficient one-pot chemoselective synthesis of nitriles from aldehydes: Mechanistic insight and selectivity control through modulation of electronic and steric factors
    • Chakraborti, A.K.; Kaur, G.; Roy, S. A simple and highly efficient one-pot chemoselective synthesis of nitriles from aldehydes: mechanistic insight and selectivity control through modulation of electronic and steric factors. Indian J. Chem. 2001, 40B, 1000-1006.
    • (2001) Indian J. Chem. , vol.40 B , pp. 1000-1006
    • Chakraborti, A.K.1    Kaur, G.2    Roy, S.3
  • 35
    • 0032171679 scopus 로고    scopus 로고
    • Efficient one pot synthesis of nitriles from aldehydes in solid state using peroxymonosulfate on alumina
    • Bose, D.S.; Narsaiah, A.V. Efficient one pot synthesis of nitriles from aldehydes in solid state using peroxymonosulfate on alumina. Tetrahedron Lett. 1998, 39, 6533-6534.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 6533-6534
    • Bose, D.S.1    Narsaiah, A.V.2
  • 36
    • 0033550250 scopus 로고    scopus 로고
    • One-pot synthesis of nitriles from aldehydes under microwave irradiation: Influence of the medium and mode of microwave irradiation on product formation
    • Chakraborti, A.K.; Kaur, G. One-pot synthesis of nitriles from aldehydes under microwave irradiation: influence of the medium and mode of microwave irradiation on product formation. Tetrahedron 1999, 55, 13265-13268.
    • (1999) Tetrahedron , vol.55 , pp. 13265-13268
    • Chakraborti, A.K.1    Kaur, G.2
  • 37
    • 84891030587 scopus 로고
    • Convenient method for conversion of aldehydes into nitriles
    • Vowinkel, E. Convenient method for conversion of aldehydes into nitriles. Angew. Chem. Intern. Ed. Engl. 1974, 13, 351-351.
    • (1974) Angew. Chem. Intern. Ed. Engl. , vol.13 , pp. 351-351
    • Vowinkel, E.1
  • 38
    • 0009294161 scopus 로고
    • Thiazoles from ethyl isocyanoacetate and thiono esters - Ethyl thiazole-4-carboxylate
    • Hartman, G.D.; Weinstock, L.M. Thiazoles from ethyl isocyanoacetate and thiono esters - ethyl thiazole-4-carboxylate. Org. Synth. 1988, 50 (9), 620-624.
    • (1988) Org. Synth. , vol.50 , Issue.9 , pp. 620-624
    • Hartman, G.D.1    Weinstock, L.M.2
  • 39
    • 0001120576 scopus 로고    scopus 로고
    • Synthesis of methyl 2-(1′,1′-dimethyl-2′-oxopropyl) thiazole-4-carboxylate and related 2,4-disubstituted thiazoles. Key intermediates in the synthesis of anthelmintic agents based on marine natural product
    • Serra, G.; Mahler, G.; Manta, E. Synthesis of methyl 2-(1′, 1′-dimethyl-2′-oxopropyl)thiazole-4-carboxylate and related 2,4-disubstituted thiazoles. Key intermediates in the synthesis of anthelmintic agents based on marine natural product. Heterocycles 1998, 48 (10), 2035-2048.
    • (1998) Heterocycles , vol.48 , Issue.10 , pp. 2035-2048
    • Serra, G.1    Mahler, G.2    Manta, E.3
  • 40
    • 0024786694 scopus 로고
    • Total synthesis of 2-(β-D-ribofuranosyl)thiazole-4-carboxamide (tiazofurin) and of precursors of ribo-C-nucleosides
    • 199
    • Bimwala, R.M.; Vogel, P. 199. Total synthesis of 2-(β-D- ribofuranosyl)thiazole-4-carboxamide (tiazofurin) and of precursors of ribo-C-nucleosides. Helv. Chim. Acta 1989, 72, 1825-1832.
    • (1989) Helv. Chim. Acta , vol.72 , pp. 1825-1832
    • Bimwala, R.M.1    Vogel, P.2
  • 41
    • 0036566861 scopus 로고    scopus 로고
    • A synthesis of a hydroxyvaline-derived thiazole-4-carboxylate constituting an antibiotic, thiocilline I
    • Yonezawa, Y.; Saito, H.; Suzuki, S.; Shin, C. A synthesis of a hydroxyvaline-derived thiazole-4-carboxylate constituting an antibiotic, thiocilline I. Heterocycles 2002, 57 (5), 903-908.
    • (2002) Heterocycles , vol.57 , Issue.5 , pp. 903-908
    • Yonezawa, Y.1    Saito, H.2    Suzuki, S.3    Shin, C.4
  • 42
    • 0002330296 scopus 로고
    • Recherches sur les dérivés du triazole-1,2,4. 3. Emploi de l'hydrazinocarbonate d'ethyle pour la synthese des hydroxy-3-triazoles-1,2,4
    • Pesson, M.; Dupin, M.S.; Antoine, M. Recherches sur les dérivés du triazole-1,2,4. 3. Emploi de l'hydrazinocarbonate d'ethyle pour la synthese des hydroxy-3-triazoles-1,2,4. Bull. Soc. Chim. Fr. 1962, 1364.
    • (1962) Bull. Soc. Chim. Fr. , pp. 1364
    • Pesson, M.1    Dupin, M.S.2    Antoine, M.3
  • 43
    • 0037446947 scopus 로고    scopus 로고
    • Performance assessment of density-functional methods for study of charge-transfer complexes
    • Liao, M.S.; Lu, Y.; Scheiner, S. Performance assessment of density-functional methods for study of charge-transfer complexes. J. Comp. Chem. 2003, 24 (5), 623-631.
    • (2003) J. Comp. Chem. , vol.24 , Issue.5 , pp. 623-631
    • Liao, M.S.1    Lu, Y.2    Scheiner, S.3
  • 44
    • 27944448251 scopus 로고    scopus 로고
    • Elliott, M., Ed.; DC, ACS: Washington
    • Elliot, M. Synthetic Pyrethroids; Elliott, M., Ed.; DC, ACS: Washington, 1997; 4-11.
    • (1997) Synthetic Pyrethroids , pp. 4-11
    • Elliot, M.1
  • 46
    • 33644811612 scopus 로고
    • A new and rapid colorimetric determination of acetylcholinesterase activity
    • Ellman, G.L.; Courtney, D.K.; Andres, V.; Featherstone, R.M. A new and rapid colorimetric determination of acetylcholinesterase activity. Biochem. Pharmacol. 1961, 7 (2), 88-95.
    • (1961) Biochem. Pharmacol. , vol.7 , Issue.2 , pp. 88-95
    • Ellman, G.L.1    Courtney, D.K.2    Andres, V.3    Featherstone, R.M.4
  • 49
    • 0000189651 scopus 로고
    • Density-functional thermochemistry. 3. The role of exact exchange
    • (a) Becke, A.D. Density-functional thermochemistry. 3. The role of exact exchange. J. Chem. Phys. 1993, 98 (7), 5648-5652;
    • (1993) J. Chem. Phys. , vol.98 , Issue.7 , pp. 5648-5652
    • Becke, A.D.1
  • 50
    • 0038596731 scopus 로고
    • Results obtained with the correlation-energy density functionals of Becke and Lee, Yang and Parr
    • (b) Miehlich, B.; Savin, A.; Stoll, H.; Preuss, H. Results obtained with the correlation-energy density functionals of Becke and Lee, Yang and Parr. Chem. Phys. Lett. 1989, 157 (3), 200-206;
    • (1989) Chem. Phys. Lett. , vol.157 , Issue.3 , pp. 200-206
    • Miehlich, B.1    Savin, A.2    Stoll, H.3    Preuss, H.4
  • 51
    • 0345491105 scopus 로고
    • Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density
    • (c) Lee, C.; Yang, W.; Parr, G. Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density. Phys. Rev. B 1988, 37(2), 785-789.
    • (1988) Phys. Rev. B , vol.37 , Issue.2 , pp. 785-789
    • Lee, C.1    Yang, W.2    Parr, G.3
  • 52
    • 0141509423 scopus 로고
    • Contracted Gaussian basis sets for molecular calculations. I. Second row atoms, Z=11-18
    • (a) McClean, A.D.; Chandler, G.S. Contracted Gaussian basis sets for molecular calculations. I. Second row atoms, Z=11-18. J. Chem. Phys. 1980, 72 (10), 5639-5648;
    • (1980) J. Chem. Phys. , vol.72 , Issue.10 , pp. 5639-5648
    • McClean, A.D.1    Chandler, G.S.2
  • 53
    • 26844534384 scopus 로고
    • Self-consistent molecular orbital methods. XX. A basis set for correlated wave functions
    • (b) Krishnan, R.; Binkley, J.S.; Seeger, R.; Pople, J.A. Self-consistent molecular orbital methods. XX. A basis set for correlated wave functions. J. Chem. Phys. 1980, 72 (1), 650-654;
    • (1980) J. Chem. Phys. , vol.72 , Issue.1 , pp. 650-654
    • Krishnan, R.1    Binkley, J.S.2    Seeger, R.3    Pople, J.A.4
  • 54
    • 0005867244 scopus 로고
    • Gaussian basis set for molecular wavefunctions containing third-row atoms
    • (c) Wachters, A.J.H. Gaussian basis set for molecular wavefunctions containing third-row atoms. J. Chem. Phys. 1970, 52 (3), 1033-1036;
    • (1970) J. Chem. Phys. , vol.52 , Issue.3 , pp. 1033-1036
    • Wachters, A.J.H.1
  • 55
    • 10144223417 scopus 로고
    • Gaussian basis sets for molecular calculations. The representation of 3d orbitals in transition-metal atoms
    • (d) Hay, P.J. Gaussian basis sets for molecular calculations. The representation of 3d orbitals in transition-metal atoms. J. Chem. Phys. 1977, 66 (10), 4377-4384;
    • (1977) J. Chem. Phys. , vol.66 , Issue.10 , pp. 4377-4384
    • Hay, P.J.1
  • 56
    • 21544443397 scopus 로고
    • Highly correlated systems. Excitation energies of first row transition metals Sc-Cu
    • (e) Raghavachari, K.; Trucks, G.W. Highly correlated systems. Excitation energies of first row transition metals Sc-Cu. J. Chem. Phys. 1989, 91 (2), 1062-1065;
    • (1989) J. Chem. Phys. , vol.91 , Issue.2 , pp. 1062-1065
    • Raghavachari, K.1    Trucks, G.W.2
  • 57
    • 36448999570 scopus 로고
    • Extension of Gaussian-2 theory to molecules containing third-row atoms Ga-Kr
    • (f) Binning, R.C.; Curtiss, L.A. Extension of Gaussian-2 theory to molecules containing third-row atoms Ga-Kr. J. Chem. Phys. 1995, 103 (14), 6104-6113;
    • (1995) J. Chem. Phys. , vol.103 , Issue.14 , pp. 6104-6113
    • Binning, R.C.1    Curtiss, L.A.2
  • 58
    • 0011414218 scopus 로고
    • Extension of Gaussian-1 (G1) theory to bromine-containing molecules
    • (g) McGrath, M.P.; Radom, L. Extension of Gaussian-1 (G1) theory to bromine-containing molecules. J. Chem. Phys. 1991, 94(1), 511-516.
    • (1991) J. Chem. Phys. , vol.94 , Issue.1 , pp. 511-516
    • McGrath, M.P.1    Radom, L.2
  • 59
    • 11744305193 scopus 로고
    • Efficient implementation of the gauge-independent atomic orbital method for NMR chemical shift calculations
    • (a) Wolinski, K.; Hilton, J.F.; Pulay, P. Efficient implementation of the gauge-independent atomic orbital method for NMR chemical shift calculations. J. Am. Chem. Soc. 1990, 112 (23), 8251-8260;
    • (1990) J. Am. Chem. Soc. , vol.112 , Issue.23 , pp. 8251-8260
    • Wolinski, K.1    Hilton, J.F.2    Pulay, P.3
  • 60
    • 84857628114 scopus 로고
    • Self-consistent perturbation-theory - Open-shell states in perturbation-dependent non-orthogonal basis-sets
    • (b) Wolinski, K.; Sadlej, A.J. Self-consistent perturbation-theory - open-shell states in perturbation-dependent non-orthogonal basis-sets. Mol. Phys. 1980, 41 (6), 1419-1430;
    • (1980) Mol. Phys. , vol.41 , Issue.6 , pp. 1419-1430
    • Wolinski, K.1    Sadlej, A.J.2
  • 61
    • 40749094858 scopus 로고
    • Self-consistent perturbation theory of diamagnetism 1. A gauge-invariant LCAO method for N.M.R. chemical shifts
    • (c) Ditchfield, R. Self-consistent perturbation theory of diamagnetism 1. A gauge-invariant LCAO method for N.M.R. chemical shifts. Mol. Phys. 1974, 27 (4), 789-807;
    • (1974) Mol. Phys. , vol.27 , Issue.4 , pp. 789-807
    • Ditchfield, R.1
  • 62
    • 33750181960 scopus 로고
    • Perturbation theory for the Fock-Dirac density matrix
    • (d) McWeeny, R. Perturbation theory for the Fock-Dirac density matrix. Phys. Rev. 1962, 126 (3), 1028-1034.
    • (1962) Phys. Rev. , vol.126 , Issue.3 , pp. 1028-1034
    • McWeeny, R.1
  • 63
    • 27944441172 scopus 로고
    • Toxicity of soil applied herbicides to brine shrimp larvae (Artemia salina) and synergism with other pesticides
    • Brighton, UK, Nov 22-25 1993BCPC Farnham: UK
    • Wilkins, R.M.; Metcalf, R.J. Toxicity of soil applied herbicides to brine shrimp larvae (Artemia salina) and synergism with other pesticides, In Proceedings of the Brighton Crop Protection Conference Weeds, Brighton, UK, Nov 22-25 1993BCPC Farnham: UK, 1993; 163-168.
    • (1993) Proceedings of the Brighton Crop Protection Conference Weeds , pp. 163-168
    • Wilkins, R.M.1    Metcalf, R.J.2
  • 64
    • 0027040713 scopus 로고
    • Insecticide resistance in Musca-domestica L from eastern England
    • Chapman, P.A.; Morgan, C.P. Insecticide resistance in Musca-domestica L from eastern England. Pesticide Sci. 1992, 36 (1), 35-45.
    • (1992) Pesticide Sci. , vol.36 , Issue.1 , pp. 35-45
    • Chapman, P.A.1    Morgan, C.P.2
  • 65
    • 0042855802 scopus 로고    scopus 로고
    • Synergistic and antagonistic interactions of anticholinesterase terpenoids in Salvia lavandulaefolia essential oil
    • Savalev, S.; Okello, E.; Perry, N.S.L.; Wilkins, R.M.; Perry, E.K. Synergistic and antagonistic interactions of anticholinesterase terpenoids in Salvia lavandulaefolia essential oil. Pharmacol. Biochem. Be. 2003, 75 (3), 661-668.
    • (2003) Pharmacol. Biochem. Be. , vol.75 , Issue.3 , pp. 661-668
    • Savalev, S.1    Okello, E.2    Perry, N.S.L.3    Wilkins, R.M.4    Perry, E.K.5


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