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Volumn 48, Issue 4, 2009, Pages 758-761

Unusual domino Michael/aldol condensation reactions employing oximes as N-selective nucleophiles: Synthesis of N-hydroxypyrroles

Author keywords

Aldehydes; Aldol reaction; Domino reactions; Michael addition; N heterocycles

Indexed keywords

ADDITION REACTIONS; ALDEHYDES; CONDENSATION; NUCLEOPHILES; ORGANIC COMPOUNDS; REACTION KINETICS;

EID: 58249112351     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200805205     Document Type: Article
Times cited : (51)

References (78)
  • 1
    • 0001275286 scopus 로고    scopus 로고
    • Eds, A. R. Katritzky, C.W. Rees, E. F. V. Scriven, Elsevier, Oxford
    • a) G. W. Gribble in Comprehensive Heterocyclic Chemistry II, Vol. 2 (Eds.: A. R. Katritzky, C.W. Rees, E. F. V. Scriven), Elsevier, Oxford, 1996, p. 207;
    • (1996) Comprehensive Heterocyclic Chemistry II , vol.2 , pp. 207
    • Gribble, G.W.1
  • 18
    • 58249109428 scopus 로고    scopus 로고
    • Examples of metal-catalyzed pyrrole syntheses: a J. T. Kim, A. V. Kel'in, V. Gevorgyan, Angew. Chem. 2003, 115, 102;
    • Examples of metal-catalyzed pyrrole syntheses: a) J. T. Kim, A. V. Kel'in, V. Gevorgyan, Angew. Chem. 2003, 115, 102;
  • 20
  • 31
    • 0037184774 scopus 로고    scopus 로고
    • Examples of metal-free pyrrole syntheses: a J. L. Bullington, R. R. Wolff, P. F. Jackson, J. Org. Chem. 2002, 67, 9439;
    • Examples of metal-free pyrrole syntheses: a) J. L. Bullington, R. R. Wolff, P. F. Jackson, J. Org. Chem. 2002, 67, 9439;
  • 43
    • 54049111906 scopus 로고    scopus 로고
    • For selected recent examples: b
    • For selected recent examples: b) B. Tan, Z. Shi, P. J. Chua, G. Zhong, Org. Lett. 2008, 10, 3425;
    • (2008) Org. Lett , vol.10 , pp. 3425
    • Tan, B.1    Shi, Z.2    Chua, P.J.3    Zhong, G.4
  • 51
  • 52
    • 33846957738 scopus 로고    scopus 로고
    • For the O-selective organocatalytic Michael addition of oximes to enals: a S. Bertelsen, P. Dinér, R. L. Johansen, K. A. Jørgensen, J. Am. Chem. Soc. 2007, 129, 1536;
    • For the O-selective organocatalytic Michael addition of oximes to enals: a) S. Bertelsen, P. Dinér, R. L. Johansen, K. A. Jørgensen, J. Am. Chem. Soc. 2007, 129, 1536;
  • 54
    • 27644519641 scopus 로고    scopus 로고
    • For a review on amination with oximes: c
    • For a review on amination with oximes: c) K. Narasaka, M. Kitamura, Eur. J. Org. Chem. 2005, 4505.
    • (2005) Eur. J. Org. Chem , pp. 4505
    • Narasaka, K.1    Kitamura, M.2
  • 55
    • 53349170687 scopus 로고    scopus 로고
    • For reviews: a
    • For reviews: a) C. F. Barbas III, Angew. Chem. 2008, 120, 44;
    • (2008) Angew. Chem , vol.120 , pp. 44
    • Barbas III, C.F.1
  • 61
    • 34247111301 scopus 로고    scopus 로고
    • Examples of iminium activation of conjugated aldehydes: f D. Enders, M. H. Bonten, G. Raabe, Synlett 2007, 0885;
    • Examples of iminium activation of conjugated aldehydes: f) D. Enders, M. H. Bonten, G. Raabe, Synlett 2007, 0885;


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.