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Volumn 11, Issue 43, 2013, Pages 7463-7466

Highly enantioselective iron(ii)-catalyzed opening reaction of aromatic meso-epoxides with indoles

Author keywords

[No Author keywords available]

Indexed keywords

CIS-STILBENE; ENANTIOSELECTIVE; INDOLE DERIVATIVES; OPENING REACTIONS;

EID: 84886937896     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c3ob41782d     Document Type: Article
Times cited : (38)

References (74)
  • 2
    • 0003445429 scopus 로고    scopus 로고
    • in, ed. E. N. Jacobsen, A. Pfaltz and H. Yamamoto, Springer, Berlin, p. 1309
    • E. N. Jacobsen and M. H. Wu, in Comprehensive Asymmetric Catalysis, ed., E. N. Jacobsen, A. Pfaltz, and, H. Yamamoto, Springer, Berlin, 1999, vol. III, p. 1309
    • (1999) Comprehensive Asymmetric Catalysis , vol.3
    • Jacobsen, E.N.1    Wu, M.H.2
  • 28
    • 0034833453 scopus 로고    scopus 로고
    • For a highly enantioselective synthesis of chiral 1,2-diols via desymmetrization of meso-epoxides using an enzymatic method, see
    • J. M. Ready E. N. Jacobsen J. Am. Chem. Soc. 2001 123 2687
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 2687
    • Ready, J.M.1    Jacobsen, E.N.2
  • 57
    • 25044437694 scopus 로고
    • in, ed. K. H. Dötz and R. W. Hoffmann, Vieweg, Braunschweig, p. 223 For reports on the use of iron catalysts in organic synthesis, see
    • C. Bolm, in Organic Synthesis via Organometallics, ed., K. H. Dötz, and, R. W. Hoffmann, Vieweg, Braunschweig, 1991, p. 223
    • (1991) Organic Synthesis Via Organometallics
    • Bolm, C.1
  • 64
    • 69249201068 scopus 로고    scopus 로고
    • II salt led to decreased yields and enantioselectivities, see
    • C. Bolm Nat. Chem. 2009 1 420
    • (2009) Nat. Chem. , vol.1 , pp. 420
    • Bolm, C.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.