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Volumn 52, Issue 46, 2011, Pages 6199-6202

Highly diastereoselective Claisen rearrangement leading to vicinal quaternary carbons construction of oxindoles

Author keywords

Cascade reactions; Isomerization; Olefination; Spirooxindoles

Indexed keywords

CARBON; INDOLE DERIVATIVE; METHYLPHOSPHONIC ACID; OXINDOLE;

EID: 80054092551     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2011.09.059     Document Type: Article
Times cited : (9)

References (49)
  • 7
    • 0003417469 scopus 로고
    • Recent reviews: B.M. Trost, Pergamon Oxford Vol. 5
    • Recent reviews: P. Wipf Comprehensive Organic Synthesis B.M. Trost, 1991 Pergamon Oxford 827 873 Vol. 5
    • (1991) Comprehensive Organic Synthesis , pp. 827-873
    • Wipf, P.1
  • 24
    • 0037423350 scopus 로고    scopus 로고
    • A few examples for assembly of vicinal quaternary carbon centers are also shown in the following reports, respectively, but their diastereoselectivities (20 or 40% de) are inadequate
    • A few examples for assembly of vicinal quaternary carbon centers are also shown in the following reports, respectively, but their diastereoselectivities (20 or 40% de) are inadequate: A.V. Novikov, A.R. Kennedy, and J.D. Rainier J. Org. Chem. 68 2003 993 996
    • (2003) J. Org. Chem. , vol.68 , pp. 993-996
    • Novikov, A.V.1    Kennedy, A.R.2    Rainier, J.D.3
  • 46
    • 0348025724 scopus 로고
    • The π-stacking interactions was suggested as the factor for the stereoselectivity in the Claisen rearrangement
    • The π-stacking interactions was suggested as the factor for the stereoselectivity in the Claisen rearrangement: J.D. White, E.G. Nolen Jr., and C.H. Miler J. Org. Chem. 51 1986 1152 1155
    • (1986) J. Org. Chem. , vol.51 , pp. 1152-1155
    • White, J.D.1    Nolen, Jr.E.G.2    Miler, C.H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.