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Volumn 45, Issue 34, 2006, Pages 5652-5655

Glycosidation promoted by a reusable solid superacid in supercritical carbon dioxide

Author keywords

Chromatography; Glycosidation; Green chemistry; Superacidic systems; Supercritical fluids

Indexed keywords

GLYCOSIDATION; GREEN CHEMISTRY; SUPERACIDIC SYSTEMS;

EID: 33748560530     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200602161     Document Type: Article
Times cited : (15)

References (42)
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    • For selected reviews on chemical glycosidation, see: a) R. R. Schmidt, Angew. Chem. 1986, 98, 213;
    • (1986) Angew. Chem. , vol.98 , pp. 213
    • Schmidt, R.R.1
  • 27
    • 25444480799 scopus 로고    scopus 로고
    • 4, AgOTf, and N-iodosuccimide/trifluoromethanesulfonic acid (NIS/TfOH) in petroleum-derived common organic solvents such as dichloromethane, dichloroethane, toluene, ether, tetrahydrofuran, and acetonitrile. As for the novel approaches in this area, see: a) K.-S. Ko, F. A. Jaipuri, N. L. Pohl, J. Am. Chem. Soc. 2005, 127, 13 162;
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 13162
    • Ko, K.-S.1    Jaipuri, F.A.2    Pohl, N.L.3
  • 30
    • 33748543765 scopus 로고    scopus 로고
    • Patent WO PCT/JP99/04261, 1999
    • a) S.-I. Nishimura, Patent WO PCT/JP99/04261, 1999;
    • Nishimura, S.-I.1
  • 41
    • 0021763991 scopus 로고
    • Compound 16 was hydrogenated and characterized as known compounds that were reported previously, see: H. A. El-Shenawy, C. Schuerch, Carbohydr. Res. 1984, 131, 227.
    • (1984) Carbohydr. Res. , vol.131 , pp. 227
    • El-Shenawy, H.A.1    Schuerch, C.2
  • 42
    • 33748534656 scopus 로고    scopus 로고
    • note
    • To achieve much higher yields and stereoselective glycosidation by using the present SCF-SFC synthesis, we are now evaluating feasibility of many other solid Lewis acid catalysts and the results will be reported shortly.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.