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Volumn 46, Issue 31, 2007, Pages 5901-5903

Palladium-catalyzed asymmetric [3+3] cycloaddition of trimethylenemethane derivatives with nitrones

Author keywords

Asymmetric catalysis; Cycloaddition; Nitrones; Palladium; Trimethylenemethanes

Indexed keywords

CATALYST ACTIVITY; CYCLOADDITION; DERIVATIVES; PALLADIUM; STEREOSELECTIVITY;

EID: 34547767107     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200701529     Document Type: Article
Times cited : (78)

References (33)
  • 4
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    • An example of the non-asymmetric variant was previously reported: R. Shintani, T. Hayashi, J. Am. Chem. Soc. 2006, 128, 6330
    • An example of the non-asymmetric variant was previously reported: R. Shintani, T. Hayashi, J. Am. Chem. Soc. 2006, 128, 6330.
  • 9
    • 0012850032 scopus 로고    scopus 로고
    • For a review, see, Eds, S. Kobayashi, K. A. Jørgensen, Wiley-VCH, Weinheim
    • For a review, see D. M. T. Chan in Cycloaddition Reactions in Organic Synthesis (Eds.: S. Kobayashi, K. A. Jørgensen), Wiley-VCH, Weinheim, 2002, p. 57.
    • (2002) Cycloaddition Reactions in Organic Synthesis , pp. 57
    • Chan, D.M.T.1
  • 16
    • 34547748975 scopus 로고    scopus 로고
    • 3 shows no reactivity.
    • 3 shows no reactivity.
  • 17
    • 34547729760 scopus 로고    scopus 로고
    • For examples of metal-catalyzed synthesis of 1,2-oxazines, see a I. S. Young, M. A. Kerr, Angew. Chem. 2003, 115, 3131;
    • For examples of metal-catalyzed synthesis of 1,2-oxazines, see a) I. S. Young, M. A. Kerr, Angew. Chem. 2003, 115, 3131;
  • 18
  • 20
    • 29144485901 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 7832;
    • (2005) Chem. Int. Ed , vol.44 , pp. 7832
    • Angew1
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    • 34547754043 scopus 로고    scopus 로고
    • Ref, 2
    • c) Ref. [2].
  • 29
    • 0037100318 scopus 로고    scopus 로고
    • The diastereomer of this compound ((S,R,R)-6c) has been reported: a) A. Duursma, A. J. Minnaard, B. L. Feringa, Tetrahedron 2002, 58, 5773;
    • The diastereomer of this compound ((S,R,R)-6c) has been reported: a) A. Duursma, A. J. Minnaard, B. L. Feringa, Tetrahedron 2002, 58, 5773;
  • 32
    • 34547815652 scopus 로고    scopus 로고
    • Alkyl-substituted nitrones are not suitable substrates under the present reaction conditions; they give little or no cycloadducts
    • Alkyl-substituted nitrones are not suitable substrates under the present reaction conditions; they give little or no cycloadducts.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.