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Volumn 52, Issue 16, 2011, Pages 1839-1841

Rapid, simple, and efficient deprotection of benzyl/benzylidene protected carbohydrates by utilization of flow chemistry

Author keywords

Benzyl benzylidene; Carbohydrates; Flow chemistry; Heterogenous catalysis; Protective groups

Indexed keywords

BENZYLIDENE DERIVATIVE; CARBOHYDRATE; FUNCTIONAL GROUP;

EID: 79952738770     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2010.12.109     Document Type: Article
Times cited : (15)

References (30)
  • 7
    • 33748932220 scopus 로고    scopus 로고
    • See, for example: Osborn, H. M. I., Ed.; Academic Press-Elsevier: Oxford
    • See, for example: (a) Robertson, J.; Stafford, P. M. Carbohydrates In Osborn, H. M. I., Ed.; Academic Press-Elsevier: Oxford, 2003. pp 9-65;
    • (2003) Carbohydrates , pp. 9-65
    • Robertson, J.1    Stafford, P.M.2
  • 10
    • 0001569822 scopus 로고
    • See, for example
    • See, for example: (a) Garegg, P. J. Acc. Chem. Res. 1992, 25, 575-580;
    • (1992) Acc. Chem. Res. , vol.25 , pp. 575-580
    • Garegg, P.J.1
  • 13
    • 0003405157 scopus 로고    scopus 로고
    • Thieme, Georg, Ed.; Verlag: Stuttgart
    • Kocieński, P. J. In Protecting Groups; Thieme, Georg, Ed.; Verlag: Stuttgart, 2005. Vol. 3, pp 137-155 and 241-257.
    • (2005) Protecting Groups , vol.3
    • Kocieński, P.J.1
  • 20
    • 0034001616 scopus 로고    scopus 로고
    • For preparation and analytical data of compounds 1-4, see for example
    • For preparation and analytical data of compounds 1-4, see for example: (a) Tennant-Eyles, R. J.; Davis, B. G.; Fairbanks, A. J. Tetrahedron: Asymmetry 2000, 11, 231-243;
    • (2000) Tetrahedron: Asymmetry , vol.11 , pp. 231-243
    • Tennant-Eyles, R.J.1    Davis, B.G.2    Fairbanks, A.J.3
  • 29
    • 0347416794 scopus 로고    scopus 로고
    • In a typical experimental setup, 20 mg of substrate was dissolved in 20 ml EtOAc:MeOH (1:1). The flow velocity was set with the HPLC pump to 1 ml/min. The hydrogen pressure was set to 40 bar, the temperature to 80 °C and a cartridge containing 10% Pd/C was utilized. After the reaction the sample was collected and evaporated to give the pure product. For analytical data on the products, see
    • In a typical experimental setup, 20 mg of substrate was dissolved in 20 ml EtOAc:MeOH (1:1). The flow velocity was set with the HPLC pump to 1 ml/min. The hydrogen pressure was set to 40 bar, the temperature to 80 °C and a cartridge containing 10% Pd/C was utilized. After the reaction the sample was collected and evaporated to give the pure product. For analytical data on the products, see: (a) Belakhov, V.; Dovgolevsky, E.; Rabkin, E.; Shulami, S.; Shoham, Y.; Baasov, T. Carbohydr. Res. 2004, 339, 385-392;
    • (2004) Carbohydr. Res. , vol.339 , pp. 385-392
    • Belakhov, V.1    Dovgolevsky, E.2    Rabkin, E.3    Shulami, S.4    Shoham, Y.5    Baasov, T.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.