메뉴 건너뛰기




Volumn 40, Issue 6, 2010, Pages 855-860

Approach to the valorization of carbohydrates as raw materials by microwave-assisted neat 1,3-dipolar cycloaddition

Author keywords

1,3 dipolar cycloaddition; Carbohydrate; Chiral auxiliary; Microwave; Neat reaction

Indexed keywords

1 O 2',3' DI PHENYL 5' METHYL ISOXAZOLIDIN 4' YL] 2,3,4 TRI O BENZOYL ALPHA XYLOPYRANOSE; 1 O 2',3' DI PHENYL 5' METHYL ISOXAZOLIDIN 4' YL] 2,3,4 TRI O BENZOYL BETA XYLOPYRANOSE; 1 O 2',3' DI PHENYL 5' METHYL ISOXAZOLIDIN 4' YL] 2,3,4,6 TETRA O ACETYL BETA GLUCOPYRANOSE; CARBOHYDRATE DERIVATIVE; METHYL 2,3,4 TRI O ACETYL 6 O 2',3' DI PHENYL 5' METHYL ISOXAZOLIDIN 4' YL]ALPHA GLUCOPYRANOSIDE; UNCLASSIFIED DRUG;

EID: 77249129939     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910903019959     Document Type: Article
Times cited : (4)

References (15)
  • 1
    • 0033693921 scopus 로고    scopus 로고
    • Cycloadditions under microwave irradiation conditions: Methods and applications
    • de la Hoz, A.; Diaz-Ortis, A.; Moreno, A.; Langa, F. Cycloadditions under microwave irradiation conditions: Methods and applications. Eur. J. Org. Chem. 2000, 3659-3673.
    • (2000) Eur. J. Org. Chem. , pp. 3659-3673
    • De La Hoz, A.1    Diaz-Ortis, A.2    Moreno, A.3    Langa, F.4
  • 3
    • 44349156193 scopus 로고    scopus 로고
    • On the energy efficiency of microwave-assisted organic reactions
    • Razzaq, T.; Kappe, C. O. On the energy efficiency of microwave-assisted organic reactions. Chem. Sus. Chem. 2008, 1, 123-132.
    • (2008) Chem. Sus. Chem. , vol.1 , pp. 123-132
    • Razzaq, T.1    Kappe, C.O.2
  • 5
    • 11544346529 scopus 로고    scopus 로고
    • Asymmetric 1,3-dipolar cycloaddition reactions
    • Gothelf, K. V.; Jørgensen, K. A. Asymmetric 1,3-dipolar cycloaddition reactions. Chem. Rev. 1998, 98, 863-909.
    • (1998) Chem. Rev. , vol.98 , pp. 863-909
    • Gothelf, K.V.1    Jørgensen, K.A.2
  • 6
    • 35548985408 scopus 로고    scopus 로고
    • Intramolecular 1,3-dipolar cycloaddition reactions in targeted syntheses
    • Nair, V.; Suja, T. D. Intramolecular 1,3-dipolar cycloaddition reactions in targeted syntheses. Tetrahedron 2007, 63, 12247-12275.
    • (2007) Tetrahedron , vol.63 , pp. 12247-12275
    • Nair, V.1    Suja, T.D.2
  • 8
    • 0035898741 scopus 로고    scopus 로고
    • [1,3]-Dipolar intramolecular nitrone olefin cycloaddition reaction of a sugar-derived a,b-unsaturated ester: A new diastereo-and regioselective synthesis of an aminocyclopentitol
    • Jachak, S. M.; Karche, N. P.; Dhavale, D. D. [1,3]-Dipolar intramolecular nitrone olefin cycloaddition reaction of a sugar-derived a,b-unsaturated ester: A new diastereo-and regioselective synthesis of an aminocyclopentitol. Tetrahedron Lett. 2001, 42, 4925-4928.
    • (2001) Tetrahedron Lett. , vol.42 , pp. 4925-4928
    • Jachak, S.M.1    Karche, N.P.2    Dhavale, D.D.3
  • 9
    • 0037377598 scopus 로고    scopus 로고
    • 1,3-Dipolar cycloadditions in the synthesis of carbohydrate mimics, part 2: Nitrones and oximes
    • Koumbis, A. E.; Gallos, J. K. 1,3-Dipolar cycloadditions in the synthesis of carbohydrate mimics, part 2: Nitrones and oximes. Curr. Org. Chem. 2003, 7, 585-628.
    • (2003) Curr. Org. Chem. , vol.7 , pp. 585-628
    • Koumbis, A.E.1    Gallos, J.K.2
  • 10
    • 37049020226 scopus 로고    scopus 로고
    • Synthesis of novel carbohydrate acridinone derivatives with potential biological activities using 1,3-dipolar cycloaddition
    • Fascio, M. L.; D'Accorso, N. B.; Pellon, R. F.; Docampo, M. L. Synthesis of novel carbohydrate acridinone derivatives with potential biological activities using 1,3-dipolar cycloaddition. Synth. Commun. 2007, 37, 4209-4217.
    • (2007) Synth. Commun. , vol.37 , pp. 4209-4217
    • Fascio, M.L.1    D'Accorso, N.B.2    Pellon, R.F.3    Docampo, M.L.4
  • 11
    • 33746316409 scopus 로고    scopus 로고
    • 1 3-Dipolar cycloaddition reactions on carbohydrate-based templates: Synthesis of spiro-isoxazolines and 1, 2,4-oxadiazoles as glycogen phosphorylase inhibitors
    • Benltifa, M.; Vidal, S.; Gueyrard, D.; Goekjian, P. G.; Msaddek, M.; Praly, J. P. 1,3-Dipolar cycloaddition reactions on carbohydrate-based templates: Synthesis of spiro-isoxazolines and 1,2,4-oxadiazoles as glycogen phosphorylase inhibitors. Tetrahedron Lett. 2006, 47, 6143-6147.
    • (2006) Tetrahedron Lett. , vol.47 , pp. 6143-6147
    • Benltifa, M.1    Vidal, S.2    Gueyrard, D.3    Goekjian, P.G.4    Msaddek, M.5    Praly, J.P.6
  • 12
    • 0036027099 scopus 로고    scopus 로고
    • 1,3-Dipolar cycloaddition reactions of carbohydrate derived nitrones and oximes
    • Osborn, H. M. I.; Gemmell, N.; Harwood, L. M. 1,3-Dipolar cycloaddition reactions of carbohydrate derived nitrones and oximes. J. Chem. Soc. Perk. Trans. 1 2002, 2419-2438.
    • (2002) J. Chem. Soc. Perk. Trans. , Issue.1 , pp. 2419-2438
    • Osborn, H.M.I.1    Gemmell, N.2    Harwood, L.M.3
  • 13
    • 53149129779 scopus 로고    scopus 로고
    • Exploiting microwave-assisted neat procedures: Synthesis of N-aryl and N-alkylnitrones and their cycloaddition en route for isoxazolidines
    • Andrade, M. M.; Barros, M. T.; Pinto, R. C. Exploiting microwave-assisted neat procedures: Synthesis of N-aryl and N-alkylnitrones and their cycloaddition en route for isoxazolidines. Tetrahedron 2008, 64, 10521-10530.
    • (2008) Tetrahedron , vol.64 , pp. 10521-10530
    • Andrade, M.M.1    Barros, M.T.2    Pinto, R.C.3
  • 14
    • 34547678621 scopus 로고    scopus 로고
    • Selective synthesis under microwave irradiation of carbohydrate derivatives containing unsaturated systems
    • Andrade, M. M.; Barros, M. T.; Rodrigues, P. Selective synthesis under microwave irradiation of carbohydrate derivatives containing unsaturated systems. Eur. J. Org. Chem. 2007, 3655-3668.
    • (2007) Eur. J. Org. Chem. , pp. 3655-3668
    • Andrade, M.M.1    Barros, M.T.2    Rodrigues, P.3
  • 15
    • 53149129779 scopus 로고    scopus 로고
    • Exploiting microwave-assisted neat procedures: Synthesis of N-aryl and N-alkylnitrones and their cycloaddition en route for isoxazolidines
    • Andrade, M. M.; Barros, M. T.; Pinto, R. C. Exploiting microwave-assisted neat procedures: Synthesis of N-aryl and N-alkylnitrones and their cycloaddition en route for isoxazolidines. Tetrahedron 2008, 64, 10521-10530.
    • (2008) Tetrahedron , vol.64 , pp. 10521-10530
    • Andrade, M.M.1    Barros, M.T.2    Pinto, R.C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.