메뉴 건너뛰기




Volumn 38, Issue 23, 2008, Pages 4240-4249

Solid-phase organic synthesis of vinyl-substituted 1,3,4-oxadiazoles using polymer-bound α-selenopropionic acid

Author keywords

Polystyrene supported selenopropionic acid; Solid phase organic synthesis; Vinyl substituted 1,3,4 oxadiazole

Indexed keywords

5 (4 CHLOROPHENYL) 2 VINYL 1,3,4 OXADIAZOLE; 5 (4 METHOXYPHENYL) 2 VINYL 1,3,4 OXADIAZOLE; 5 (4 NITROPHENYL) 2 VINYL 1,3,4 OXADIAZOLE; 5 (ISOPROPYL) 2 VINYL 1,3,4 OXADIAZOLE; 5 (N HEXYL) 2 VINYL 1,3,4 OXADIAZOLE; 5 BENZYL 2 VINYL 1,3,4 OXADIAZOLE; 5 PHENYL 2 VINYL 1,3,4 OXADIAZOLE; OXADIAZOLE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 55349116751     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910802324518     Document Type: Article
Times cited : (8)

References (49)
  • 1
    • 0036436990 scopus 로고    scopus 로고
    • Solid phase heterocyclic chemistry
    • For reviews on synthesis of heterocycles, see a
    • (a) For reviews on synthesis of heterocycles, see (a) Krchňák, V.; Holladay, M. W. Solid phase heterocyclic chemistry. Chem. Rev. 2002, 102(1), 61-92;
    • (2002) Chem. Rev , vol.102 , Issue.1 , pp. 61-92
    • Krchňák, V.1    Holladay, M.W.2
  • 2
    • 0041037814 scopus 로고    scopus 로고
    • Recent advances in the preparation of heterocycles on solid support: A review of the literature
    • (b) Franzèn, R. G. Recent advances in the preparation of heterocycles on solid support: A review of the literature. J. Comb. Chem. 2000, 2(3), 195-214;
    • (2000) J. Comb. Chem , vol.2 , Issue.3 , pp. 195-214
    • Franzèn, R.G.1
  • 3
    • 0037366605 scopus 로고    scopus 로고
    • The combinatorial synthesis of bicyclic privileged structures or privileged substructures
    • (c) Horton, D. A.; Bourne, G. T.; Smythe, M. L. The combinatorial synthesis of bicyclic privileged structures or privileged substructures. Chem. Rev. 2003, 103(3), 893-930.
    • (2003) Chem. Rev , vol.103 , Issue.3 , pp. 893-930
    • Horton, D.A.1    Bourne, G.T.2    Smythe, M.L.3
  • 4
    • 0025816212 scopus 로고
    • 2-(Oxadiazolyl)-and 2-(thiazolyl)imidazo[1,2-a]pyrimidines as agonists and inverse agonists at benzodiazepine receptors
    • (a) Tully, W. R.; Cardner, C. R.; Gillespie, R. J.; Westwood, R. 2-(Oxadiazolyl)-and 2-(thiazolyl)imidazo[1,2-a]pyrimidines as agonists and inverse agonists at benzodiazepine receptors. J. Med. Chem. 1991, 34(7), 2060-2067;
    • (1991) J. Med. Chem , vol.34 , Issue.7 , pp. 2060-2067
    • Tully, W.R.1    Cardner, C.R.2    Gillespie, R.J.3    Westwood, R.4
  • 5
    • 0027938648 scopus 로고
    • Improved Fischer indole reaction for the preparation of N,N-dimethyltryptamines: Synthesis of L-695, 894, a potent 5-HT1D receptor agonist
    • (b) Chen, C. Y.; Senanayake, C. H.; Bill, T. J.; Larsen, R. D.; Veshoeven, T. R.; Reider, P. J. Improved Fischer indole reaction for the preparation of N,N-dimethyltryptamines: Synthesis of L-695, 894, a potent 5-HT1D receptor agonist. J. Org. Chem. 1994, 59(13), 3738-3741;
    • (1994) J. Org. Chem , vol.59 , Issue.13 , pp. 3738-3741
    • Chen, C.Y.1    Senanayake, C.H.2    Bill, T.J.3    Larsen, R.D.4    Veshoeven, T.R.5    Reider, P.J.6
  • 6
    • 0036318617 scopus 로고    scopus 로고
    • Synthesis of new 2,5-disubstituted-1,3,4-thiadiazoles and preliminary evaluation of anticonvulsant and antimicrobial activities
    • (c) Dogan, H. N.; Duran, A.; Rollas, S.; Sener, G.; Uysal, M. K.; Gülen, D. Synthesis of new 2,5-disubstituted-1,3,4-thiadiazoles and preliminary evaluation of anticonvulsant and antimicrobial activities. Bioorg. Med. Chem. 2002, 10(9), 2893-3898.
    • (2002) Bioorg. Med. Chem , vol.10 , Issue.9 , pp. 2893-3898
    • Dogan, H.N.1    Duran, A.2    Rollas, S.3    Sener, G.4    Uysal, M.K.5    Gülen, D.6
  • 7
    • 0035138869 scopus 로고    scopus 로고
    • Synthesis and quantitative structure-activity relationships of new 2,5-disubstituted-1,3,4-oxadiazoles
    • (a) Shi, W.; Qian, X.; Zhang, R.; Song, G. Synthesis and quantitative structure-activity relationships of new 2,5-disubstituted-1,3,4-oxadiazoles. J. Agric. Food Chem. 2001, 49(1), 124-130;
    • (2001) J. Agric. Food Chem , vol.49 , Issue.1 , pp. 124-130
    • Shi, W.1    Qian, X.2    Zhang, R.3    Song, G.4
  • 8
    • 0033661951 scopus 로고    scopus 로고
    • Synthesis and fungicidal activity against Rhizoctonia solani of 2-alkyl (alkylthio)-5-pyrazolyl-1,3,4-oxadiazoles (thiadiazoles)
    • (b) Chen, H.; Li, Z.; Han, Y. Synthesis and fungicidal activity against Rhizoctonia solani of 2-alkyl (alkylthio)-5-pyrazolyl-1,3,4-oxadiazoles (thiadiazoles). J. Agric. Food Chem. 2000, 48(11), 5312-5315.
    • (2000) J. Agric. Food Chem , vol.48 , Issue.11 , pp. 5312-5315
    • Chen, H.1    Li, Z.2    Han, Y.3
  • 9
    • 0034733114 scopus 로고    scopus 로고
    • Novel photoluminescent polymers containing oligothiophene and m-phenylene-1,3,4-oxadiazole moieties: Synthesis and spectroscopic and electrochemical studies
    • (a) Meng, H.; Huang, W. Novel photoluminescent polymers containing oligothiophene and m-phenylene-1,3,4-oxadiazole moieties: Synthesis and spectroscopic and electrochemical studies. J. Org. Chem. 2000, 65(13), 3894-3901;
    • (2000) J. Org. Chem , vol.65 , Issue.13 , pp. 3894-3901
    • Meng, H.1    Huang, W.2
  • 10
    • 0035124222 scopus 로고    scopus 로고
    • Synthesis, characterization, and study of the thermal properties of new poly(arylene ether 1,3,4-oxadiazole) s
    • (b) Bottino, F. A.; Pasquale, G. D.; Iannelli, P. Synthesis, characterization, and study of the thermal properties of new poly(arylene ether 1,3,4-oxadiazole) s. Macromolecules 2001, 34(1), 33-37;
    • (2001) Macromolecules , vol.34 , Issue.1 , pp. 33-37
    • Bottino, F.A.1    Pasquale, G.D.2    Iannelli, P.3
  • 11
    • 0032636345 scopus 로고    scopus 로고
    • Photoluminescent poly(p-phenylenevinylene)s with an aromatic oxadiazole moiety as the side shain: Synthesis, slectrochemistry, and spectroscopy study
    • (c) Chen, Z.-K.; Meng, H.; Lai; Y.-H.; Huang, W. Photoluminescent poly(p-phenylenevinylene)s with an aromatic oxadiazole moiety as the side shain: Synthesis, slectrochemistry, and spectroscopy study. Macromolecules 1999, 32(13), 4351-4358.
    • (1999) Macromolecules , vol.32 , Issue.13 , pp. 4351-4358
    • Chen, Z.-K.1    Meng, H.2    Lai, Y.-H.3    Huang, W.4
  • 12
    • 0000679775 scopus 로고
    • Synthesis of multidentate 1,3,4-oxadiazole-, imine-, and phenol-containing macrocycles
    • (a) Perez, M. A.; Bermejo, J. M. Synthesis of multidentate 1,3,4-oxadiazole-, imine-, and phenol-containing macrocycles. J. Org. Chem. 1993, 58(9), 2628-2630;
    • (1993) J. Org. Chem , vol.58 , Issue.9 , pp. 2628-2630
    • Perez, M.A.1    Bermejo, J.M.2
  • 13
    • 0035095504 scopus 로고    scopus 로고
    • Luminescence properties of structurally modified PPVs: PPV derivatives bearing 2-(4-tert-butylphenyl)-5-phenyl-1,3,4-oxadiazole pendants
    • (b) Lee, D. W.; Kwon, K.-Y.; Jin, J.-I.; Park, Y.; Kim, Y.-R.; Hwang, I.-W. Luminescence properties of structurally modified PPVs: PPV derivatives bearing 2-(4-tert-butylphenyl)-5-phenyl-1,3,4-oxadiazole pendants. Chem. Mater. 2001, 13(2), 565-574.
    • (2001) Chem. Mater , vol.13 , Issue.2 , pp. 565-574
    • Lee, D.W.1    Kwon, K.-Y.2    Jin, J.-I.3    Park, Y.4    Kim, Y.-R.5    Hwang, I.-W.6
  • 14
    • 0033574569 scopus 로고    scopus 로고
    • Novel procedure for the synthesis of 1,3,4-oxadiazoles from 1,2-diacylhydrazines using polymer-supported Burgess reagent under microwave conditions
    • For some recent examples, see a
    • For some recent examples, see (a) Brain, C. T.; Paul, J. M.; Loong, Y.; Oakley, P. J. Novel procedure for the synthesis of 1,3,4-oxadiazoles from 1,2-diacylhydrazines using polymer-supported Burgess reagent under microwave conditions. Tetrahedron Lett. 1999, 40(16), 3275-3278;
    • (1999) Tetrahedron Lett , vol.40 , Issue.16 , pp. 3275-3278
    • Brain, C.T.1    Paul, J.M.2    Loong, Y.3    Oakley, P.J.4
  • 15
    • 0033978534 scopus 로고    scopus 로고
    • Brown, B. J.; Clemens, I. R.; Neesom, J. K. Diisopropylcarbodiimide: A novel reagent for the synthesis of 1,3,4-oxadiazoles on solid-phase. Synlett 2000, 1, 131-133;
    • (b) Brown, B. J.; Clemens, I. R.; Neesom, J. K. Diisopropylcarbodiimide: A novel reagent for the synthesis of 1,3,4-oxadiazoles on solid-phase. Synlett 2000, 1, 131-133;
  • 16
    • 0033975981 scopus 로고    scopus 로고
    • A mild method for the preparation of 1,3,4-oxadiazoles: Triflic anhydride promoted cyclization of diacylhydrazines
    • (c) Liras, S.; Allen, M. P.; Segelstein, B. E. A mild method for the preparation of 1,3,4-oxadiazoles: Triflic anhydride promoted cyclization of diacylhydrazines. Synth. Commun. 2000, 30(3), 437-443;
    • (2000) Synth. Commun , vol.30 , Issue.3 , pp. 437-443
    • Liras, S.1    Allen, M.P.2    Segelstein, B.E.3
  • 17
    • 0035103203 scopus 로고    scopus 로고
    • Synthesis of 1,3,4-oxadiazoles using polymer-supported reagents
    • (d) Brain, C. T.; Brunton, S. A. Synthesis of 1,3,4-oxadiazoles using polymer-supported reagents. Synlett 2001, 3, 382-384;
    • (2001) Synlett , vol.3 , pp. 382-384
    • Brain, C.T.1    Brunton, S.A.2
  • 18
    • 1642603923 scopus 로고    scopus 로고
    • Efficient one-pot preparation of 5-substituted-2-amino-1, 3, 4-oxadiazoles using resin-bound reagents
    • (e) Coppo, F. T.; Evans, K. A.; Graybill, T. L.; Burton, G. Efficient one-pot preparation of 5-substituted-2-amino-1, 3, 4-oxadiazoles using resin-bound reagents. Tetrahedron Lett. 2004, 45(16), 3257-3260;
    • (2004) Tetrahedron Lett , vol.45 , Issue.16 , pp. 3257-3260
    • Coppo, F.T.1    Evans, K.A.2    Graybill, T.L.3    Burton, G.4
  • 19
    • 18844454506 scopus 로고    scopus 로고
    • The rapid preparation of 2-aminosulfonamide-1,3,4-oxadiazoles using polymer-supported reagents and microwave heating
    • (f) Baxendale, I. R.; Ley, S. V.; Martinelli, M. The rapid preparation of 2-aminosulfonamide-1,3,4-oxadiazoles using polymer-supported reagents and microwave heating. Tetrahedron 2005, 61(22), 5323-5349;
    • (2005) Tetrahedron , vol.61 , Issue.22 , pp. 5323-5349
    • Baxendale, I.R.1    Ley, S.V.2    Martinelli, M.3
  • 20
    • 15244356346 scopus 로고    scopus 로고
    • Oxidative cyclization of aldazines with bis(trifluoroacetoxy)iodobenzene
    • (g) Shang, Z.; Reiner, J.; Chang, J.; Zhao, K. Oxidative cyclization of aldazines with bis(trifluoroacetoxy)iodobenzene. Tetrahedron Lett. 2005, 46(15), 2701-2704;
    • (2005) Tetrahedron Lett , vol.46 , Issue.15 , pp. 2701-2704
    • Shang, Z.1    Reiner, J.2    Chang, J.3    Zhao, K.4
  • 21
    • 33747772445 scopus 로고    scopus 로고
    • Facile procedure for the one-pot synthesis of unsymmetrical 2,5-disubstituted 1,3,4-oxadiazoles
    • (h) Dabiri, M.; Salehi, P.; Baghbanzadeh, M.; Bahramnejad, M. Facile procedure for the one-pot synthesis of unsymmetrical 2,5-disubstituted 1,3,4-oxadiazoles. Tetrahedron Lett. 2006, 47(39), 6983-6986.
    • (2006) Tetrahedron Lett , vol.47 , Issue.39 , pp. 6983-6986
    • Dabiri, M.1    Salehi, P.2    Baghbanzadeh, M.3    Bahramnejad, M.4
  • 22
    • 28544450601 scopus 로고    scopus 로고
    • A simple and efficient one step synthesis of 1,3,4-oxadiazoles utilizing polymer-supported reagents and microwave heating
    • (a) Wang, Y.; Sauer, D. R.; Djuric, S. W. A simple and efficient one step synthesis of 1,3,4-oxadiazoles utilizing polymer-supported reagents and microwave heating. Tetrahedron Lett. 2006, 47(1), 105-108;
    • (2006) Tetrahedron Lett , vol.47 , Issue.1 , pp. 105-108
    • Wang, Y.1    Sauer, D.R.2    Djuric, S.W.3
  • 23
    • 33748545632 scopus 로고    scopus 로고
    • 1,3,4-Oxadiazole formation as traceless release in solid phase organic synthesis
    • (b) Cesarini, S.; Colombo, N.; Pulici, M.; Felder, E. R.; Brill, W. K.-D. 1,3,4-Oxadiazole formation as traceless release in solid phase organic synthesis. Tetrahedron 2006, 62(43), 10223-10236.
    • (2006) Tetrahedron , vol.62 , Issue.43 , pp. 10223-10236
    • Cesarini, S.1    Colombo, N.2    Pulici, M.3    Felder, E.R.4    Brill, W.K.-D.5
  • 24
  • 25
    • 0034624685 scopus 로고    scopus 로고
    • Genin, M. J.; Allwine, D. A.; Anderson, D. J.; Barbachyn, M. R.; Emmert, D. E.; Garmon, S. A.; Graber, D. R.; Grega, K. C.; Hester, J. B.; Hutchinson, D. K.; Morris, J.; Reischer, R. J.; Ford, C. W.; Zurenko, G. E.; Hamel, J. C.; Schaadt, R. D.; Stapert; D.; Yagi, B. H. Substituent effects on the antibacterial activity of nitrogen-carbon-linked (azolylphenyl) oxazolidinones with expanded activity against the fastidious gram-negative organisms haemophilus influenzae and moraxella catarrhalis. J. Med. Chem. 2000, 43(5), 953-970.
    • (b) Genin, M. J.; Allwine, D. A.; Anderson, D. J.; Barbachyn, M. R.; Emmert, D. E.; Garmon, S. A.; Graber, D. R.; Grega, K. C.; Hester, J. B.; Hutchinson, D. K.; Morris, J.; Reischer, R. J.; Ford, C. W.; Zurenko, G. E.; Hamel, J. C.; Schaadt, R. D.; Stapert; D.; Yagi, B. H. Substituent effects on the antibacterial activity of nitrogen-carbon-linked (azolylphenyl) oxazolidinones with expanded activity against the fastidious gram-negative organisms haemophilus influenzae and moraxella catarrhalis. J. Med. Chem. 2000, 43(5), 953-970.
  • 26
    • 27144530628 scopus 로고    scopus 로고
    • Fine tuning the purity of blue emission from polydioctylfluorene by end-capping with electron-deficient moieties
    • (a) Hung, M. C.; Liao, J. L.; Chen, S. A.; Chen, S. H.; Su, A. C. Fine tuning the purity of blue emission from polydioctylfluorene by end-capping with electron-deficient moieties. J. Am. Chem. Soc. 2005, 127(42), 14576-14577.
    • (2005) J. Am. Chem. Soc , vol.127 , Issue.42 , pp. 14576-14577
    • Hung, M.C.1    Liao, J.L.2    Chen, S.A.3    Chen, S.H.4    Su, A.C.5
  • 27
    • 12944330024 scopus 로고    scopus 로고
    • Facile synthetic route to a novel electroluminescent polymer-poly (p-phenylenevinylene) containing a fully conjugated aromatic oxadiazole side chain
    • (b) Meng, H.; Yu, W. L.; Huang, W. Facile synthetic route to a novel electroluminescent polymer-poly (p-phenylenevinylene) containing a fully conjugated aromatic oxadiazole side chain. Macromolecules 1999, 32(26), 8841-8847.
    • (1999) Macromolecules , vol.32 , Issue.26 , pp. 8841-8847
    • Meng, H.1    Yu, W.L.2    Huang, W.3
  • 29
    • 34347247220 scopus 로고    scopus 로고
    • An efficient route to vinyl substituted oxadiazoles and triazoles using phenylselanyl derivatives as precursor
    • Wang, Y.-G.; Huang, X.; Wu, Y.-Z. An efficient route to vinyl substituted oxadiazoles and triazoles using phenylselanyl derivatives as precursor. Tetrahedron 2007, 63(33), 7866-7873.
    • (2007) Tetrahedron , vol.63 , Issue.33 , pp. 7866-7873
    • Wang, Y.-G.1    Huang, X.2    Wu, Y.-Z.3
  • 30
    • 0002389988 scopus 로고
    • Functional group manipulation using organoselenium reagents
    • (a) Reich, H. J. Functional group manipulation using organoselenium reagents. Acc. Chem. Res. 1979, 12(1), 22-30;
    • (1979) Acc. Chem. Res , vol.12 , Issue.1 , pp. 22-30
    • Reich, H.J.1
  • 32
    • 0004112606 scopus 로고
    • Liotta, D, Ed, Wiley: New York
    • (c) Liotta, D. (Ed.). Organoselenium Chemistry; Wiley: New York, 1987;
    • (1987) Organoselenium Chemistry
  • 33
    • 0004112604 scopus 로고    scopus 로고
    • Oxford University Press: Oxford
    • (d) Back, T. G. Organoselenium Chemistry; Oxford University Press: Oxford, 1999; pp. 173-191;
    • (1999) Organoselenium Chemistry , pp. 173-191
    • Back, T.G.1
  • 35
    • 0000853567 scopus 로고    scopus 로고
    • Polymer-supported selenium reagents for organic synthesis
    • (a) Nicolaou, K. C.; Pastor, J.; Barluenga, S.; Winssinger, N. Polymer-supported selenium reagents for organic synthesis. Chem. Commun. 1998, 18), 1947-1948;
    • (1998) Chem. Commun , vol.18 , pp. 1947-1948
    • Nicolaou, K.C.1    Pastor, J.2    Barluenga, S.3    Winssinger, N.4
  • 36
    • 0032509385 scopus 로고    scopus 로고
    • Selenium-linking strategy for traceless solid-phase synthesis: Direct loading, aliphatic C-H bond formation upon cleavage and reaction monitoring by gradient MAS NMR spectroscopy
    • (b) Ruhland, T.; Andersen, K.; Pedersen, H. Selenium-linking strategy for traceless solid-phase synthesis: Direct loading, aliphatic C-H bond formation upon cleavage and reaction monitoring by gradient MAS NMR spectroscopy. J. Org. Chem. 1998, 63(25), 9204-9211;
    • (1998) J. Org. Chem , vol.63 , Issue.25 , pp. 9204-9211
    • Ruhland, T.1    Andersen, K.2    Pedersen, H.3
  • 37
    • 0035818026 scopus 로고    scopus 로고
    • Novel polymer-bound chiral selenium electrophiles
    • (c) Uehlin, L.; Wirth, T. Novel polymer-bound chiral selenium electrophiles. Org. Lett. 2001, 3(18), 2931-2933;
    • (2001) Org. Lett , vol.3 , Issue.18 , pp. 2931-2933
    • Uehlin, L.1    Wirth, T.2
  • 38
    • 0037420761 scopus 로고    scopus 로고
    • Intramolecular oxyselenenylation and deselenenylation reactions in water, conducted by employing polymer-supported arylselenenyl bromide
    • (d) Fujita, K.-I.; Hashimoto, S.; Oishi, A.; Taguchi, Y. Intramolecular oxyselenenylation and deselenenylation reactions in water, conducted by employing polymer-supported arylselenenyl bromide. Tetrahedron Lett. 2003, 44(19), 3793-3795;
    • (2003) Tetrahedron Lett , vol.44 , Issue.19 , pp. 3793-3795
    • Fujita, K.-I.1    Hashimoto, S.2    Oishi, A.3    Taguchi, Y.4
  • 39
    • 0142196886 scopus 로고    scopus 로고
    • Radical carbonylation/reductive cyclization for the construction of tetrahydrofuran-3-ones and pyrrolidin-3-ones
    • (e) Berlin, S.; Ericsson, C.; Engman, L. Radical carbonylation/reductive cyclization for the construction of tetrahydrofuran-3-ones and pyrrolidin-3-ones. J. Org. Chem. 2003, 68(22), 8386-8396;
    • (2003) J. Org. Chem , vol.68 , Issue.22 , pp. 8386-8396
    • Berlin, S.1    Ericsson, C.2    Engman, L.3
  • 40
    • 2942596053 scopus 로고    scopus 로고
    • A novel and highly efficient synthetic route to unsymmetrical organoselenides using cesium bases
    • (f) Cohen, R. J.; Fox, D. L.; Salvatore, R. N. A novel and highly efficient synthetic route to unsymmetrical organoselenides using cesium bases. J. Org. Chem. 2004, 69(12), 4265-4268.
    • (2004) J. Org. Chem , vol.69 , Issue.12 , pp. 4265-4268
    • Cohen, R.J.1    Fox, D.L.2    Salvatore, R.N.3
  • 41
    • 0141675017 scopus 로고    scopus 로고
    • Huang, X.; Sheng, S.-R. A facile solid-phase synthesis of substituted 2 (5H)-furanones from polymer-supported a-selenocarboxylic acids. J. Comb. Chem. 2003, 5(3), 273-277;
    • (a) Huang, X.; Sheng, S.-R. A facile solid-phase synthesis of substituted 2 (5H)-furanones from polymer-supported a-selenocarboxylic acids. J. Comb. Chem. 2003, 5(3), 273-277;
  • 42
    • 0035905089 scopus 로고    scopus 로고
    • Reactions of aldehydes with polymer-supported selenoalkylidenetriphenyl-phosphoranes: A facile method for the synthesis of carbonyl compound
    • (b) Huang, X.; Sheng S.-R. Reactions of aldehydes with polymer-supported selenoalkylidenetriphenyl-phosphoranes: A facile method for the synthesis of carbonyl compound. Tetrahedron Lett. 2001, 42(51), 9035-9037;
    • (2001) Tetrahedron Lett , vol.42 , Issue.51 , pp. 9035-9037
    • Huang, X.1    Sheng, S.-R.2
  • 43
    • 33746636878 scopus 로고    scopus 로고
    • Traceless solid-phase synthesis of 3-substituted isoxazoles and 3-substituted 5-iodoisoxazolines using polystyrene-supported vinyl selenide
    • (c) Sheng, S.-R.; Xin, Q.; Liu, X.-L.; Sun, W.-K.; Guo, R.; Huang, X. Traceless solid-phase synthesis of 3-substituted isoxazoles and 3-substituted 5-iodoisoxazolines using polystyrene-supported vinyl selenide. Synthesis 2006, 14, 2293-2296;
    • (2006) Synthesis , vol.14 , pp. 2293-2296
    • Sheng, S.-R.1    Xin, Q.2    Liu, X.-L.3    Sun, W.-K.4    Guo, R.5    Huang, X.6
  • 44
    • 34249010857 scopus 로고    scopus 로고
    • Solid-phase synthesis of 3-hydroxy-2-methylenealkanoates and their derivatives using polymer-supported α-phenylselenopropionate
    • (d) Sheng, S.-R.; Huang, F.-F.; Lin, S.-Y.; Liu, X.-L.; Huang, X. Solid-phase synthesis of 3-hydroxy-2-methylenealkanoates and their derivatives using polymer-supported α-phenylselenopropionate. Synthesis 2007, 9, 1373-1377;
    • (2007) Synthesis , vol.9 , pp. 1373-1377
    • Sheng, S.-R.1    Huang, F.-F.2    Lin, S.-Y.3    Liu, X.-L.4    Huang, X.5
  • 45
    • 10644248353 scopus 로고    scopus 로고
    • Polymer-supported β-bromoethyl selenide: An efficient reagent for the synthesis of aryl vinyl ethers
    • (e) Sheng, S.-R.; Liu, X.-L.; Wang, X.-C.; Xin, Q.; Song, C.-S. Polymer-supported β-bromoethyl selenide: An efficient reagent for the synthesis of aryl vinyl ethers. Synthesis 2004, 17, 2833-2836;
    • (2004) Synthesis , vol.17 , pp. 2833-2836
    • Sheng, S.-R.1    Liu, X.-L.2    Wang, X.-C.3    Xin, Q.4    Song, C.-S.5
  • 46
    • 31744445588 scopus 로고    scopus 로고
    • A facile solid-phase synthesis of aliphatic aldehydes using novel polymer-supported phenylselenomethyltrimethylsilane
    • (f) Sheng, S.-R.; Wang, Q.-Y.; Huang, Y.-X.; Xin, Q.; Liu, X.-L. A facile solid-phase synthesis of aliphatic aldehydes using novel polymer-supported phenylselenomethyltrimethylsilane. Synth. Commun. 2006, 36(4), 429-434.
    • (2006) Synth. Commun , vol.36 , Issue.4 , pp. 429-434
    • Sheng, S.-R.1    Wang, Q.-Y.2    Huang, Y.-X.3    Xin, Q.4    Liu, X.-L.5
  • 47
    • 33947291827 scopus 로고
    • Solid-phase synthesis of oligosaccharides, I: Preparation of the solid support poly[p-(1-propen-3-ol-1-yl)styrene]
    • Schuerch, C.; Frechet, J. M. Solid-phase synthesis of oligosaccharides, I: Preparation of the solid support poly[p-(1-propen-3-ol-1-yl)styrene]. J. Am. Chem. Soc. 1971, 93(2), 492-496.
    • (1971) J. Am. Chem. Soc , vol.93 , Issue.2 , pp. 492-496
    • Schuerch, C.1    Frechet, J.M.2
  • 48
    • 0033578789 scopus 로고    scopus 로고
    • 2-Chloro-1,3-dimethylimidazolinium chloride, 2: Its application to the construction of heterocycles through dehydration reactions
    • Isobe, T.; Ishikawa, T. 2-Chloro-1,3-dimethylimidazolinium chloride, 2: Its application to the construction of heterocycles through dehydration reactions. J. Org. Chem. 1999, 64(19), 6989-6992.
    • (1999) J. Org. Chem , vol.64 , Issue.19 , pp. 6989-6992
    • Isobe, T.1    Ishikawa, T.2
  • 49
    • 84981812467 scopus 로고
    • Hydration structure and intermolecular interaction in polyelectrolytes
    • Zundel, G. Hydration structure and intermolecular interaction in polyelectrolytes. Angew. Chem., Int. Ed. Engl. 1969, 8(7), 499-509.
    • (1969) Angew. Chem., Int. Ed. Engl , vol.8 , Issue.7 , pp. 499-509
    • Zundel, G.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.