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Volumn 9, Issue 1, 2005, Pages 1-29

Asymmetric ring opening of epoxides

Author keywords

[No Author keywords available]

Indexed keywords

SYNTHESIS (CHEMICAL);

EID: 11444266045     PISSN: 13852728     EISSN: None     Source Type: Journal    
DOI: 10.2174/1385272053369385     Document Type: Review
Times cited : (155)

References (122)
  • 1
    • 0000073548 scopus 로고
    • Trost, B. M.; Fleming, I, Eds.; Pergamon Press: Oxford
    • Rao, A. S. In Comprehensive Organic Synthesis; Trost, B. M.; Fleming, I, Eds.; Pergamon Press: Oxford, 1991; Vol. 7, pp. 357-387.
    • (1991) Comprehensive Organic Synthesis , vol.7 , pp. 357-387
    • Rao, A.S.1
  • 2
    • 0042883849 scopus 로고    scopus 로고
    • For recent advances in olefin epoxidation using methylrhenium trioxide as catalyst, see:
    • For recent advances in olefin epoxidation using methylrhenium trioxide as catalyst, see: Saladino, R.; Neri, V.; Pelliccia, A. R.; Mincione, E. Tetrahedron 2003, 59, 7403.
    • (2003) Tetrahedron , vol.59 , pp. 7403
    • Saladino, R.1    Neri, V.2    Pelliccia, A.R.3    Mincione, E.4
  • 7
    • 0000096835 scopus 로고    scopus 로고
    • Epoxides can be considered as "spring-loaded" ring for nucleophilic opening
    • Epoxides can be considered as "spring-loaded" ring for nucleophilic opening: Kolb, H. C.; Finn, M. G.; Sharpless, K. B. Angew. Chem. Int. Ed. 2001, 40, 2004.
    • (2001) Angew Chem. Int. Ed. , vol.40 , pp. 2004
    • Kolb, H.C.1    Finn, M.G.2    Sharpless, K.B.3
  • 11
    • 0029118416 scopus 로고
    • For some examples of using azido compounds
    • see
    • For some examples of using azido compounds, see: Adolfsson, H.; Moberg, C. Tetrahedron: Asymmetry 1995, 6, 2023.
    • (1995) Tetrahedron: Asymmetry , vol.6 , pp. 2023
    • Adolfsson, H.1    Moberg, C.2
  • 33
    • 0345514844 scopus 로고
    • Anthracycline antibiotics are used most often in antitumor combination chemotherapy: Neidle, S
    • Anthracycline antibiotics are used most often in antitumor combination chemotherapy: Neidle, S. Nature 1977, 268, 195.
    • (1977) Nature , vol.268 , pp. 195
  • 46
    • 0033935279 scopus 로고    scopus 로고
    • For a review, see
    • For a review, see: Feringa, B. L. Acc. Chem. Res. 2000, 33, 346.
    • (2000) Acc. Chem. Res. , vol.33 , pp. 346
    • Feringa, B.L.1
  • 52
    • 46549104605 scopus 로고
    • Diol monoether can be converted into the 1,2-diol by treatment with ammonium cerium(IV) nitrate (CAN)
    • Diol monoether can be converted into the 1,2-diol by treatment with ammonium cerium(IV) nitrate (CAN): Fukuyama, T.; Laird, A. A.; Hotchkiss, L. M. Tetrahedron Lett. 1985, 26, 6291.
    • (1985) Tetrahedron Lett. , vol.26 , pp. 6291
    • Fukuyama, T.1    Laird, A.A.2    Hotchkiss, L.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.