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Volumn 49, Issue 50, 2010, Pages 9725-9729

Enantioselective synthesis of isoindolines: An organocatalyzed domino process based on the aza-Morita-Baylis-Hillman reaction

Author keywords

asymmetric catalysis; aza Michael addition; domino reactions; isoindolines; organocatalysis

Indexed keywords

ASYMMETRIC CATALYSIS; AZA-MICHAEL ADDITION; DOMINO REACTIONS; ISOINDOLINES; ORGANOCATALYSIS;

EID: 78650148583     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201004547     Document Type: Article
Times cited : (109)

References (78)
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    • For recent reviews on secondary amine catalysis, see
    • For recent reviews on secondary amine catalysis, see
  • 9
    • 78650083428 scopus 로고    scopus 로고
    • For recent reviews on Brønsted acid, Brønsted acid-base catalysis, see
    • For recent reviews on Brønsted acid, Brønsted acid-base catalysis, see
  • 17
    • 78650119538 scopus 로고    scopus 로고
    • For recent reviews on organocatalytic enantioselective domino reactions, see
    • For recent reviews on organocatalytic enantioselective domino reactions, see
  • 24
    • 78650120127 scopus 로고    scopus 로고
    • For recent reviews on the aza-Morita-Baylis-Hillman reaction, see
    • For recent reviews on the aza-Morita-Baylis-Hillman reaction, see
  • 59
    • 70349280084 scopus 로고    scopus 로고
    • Although a number of attractive domino reactions involving achiral aza-MBH process have been developed, the desired products were generally formed along with side-products owing to the complicated aza-MBH sequence
    • Although a number of attractive domino reactions involving achiral aza-MBH process have been developed, the desired products were generally formed along with side-products owing to the complicated aza-MBH sequence, see:, G.-N. Ma, J.-J. Jiang, M. Shi, Y. Wei, Chem. Commun. 2009, 5496.
    • (2009) Chem. Commun. , pp. 5496
    • Ma, G.-N.1    Jiang, J.-J.2    Shi, M.3    Wei, Y.4
  • 74
    • 78650157912 scopus 로고    scopus 로고
    • Solvent effects were crucial factors to help accelerate the domino reaction without formation of undesired aza-MBH adducts 4 (see the Supporting Information).
    • Solvent effects were crucial factors to help accelerate the domino reaction without formation of undesired aza-MBH adducts 4 (see the Supporting Information).
  • 75
    • 78650091256 scopus 로고    scopus 로고
    • The addition of M.S. (3 Å or 4 Å) was beneficial to suppress the decomposition of moisture sensitive N-tosylimines 2 (see the Supporting Information).
    • The addition of M.S. (3 Å or 4 Å) was beneficial to suppress the decomposition of moisture sensitive N-tosylimines 2 (see the Supporting Information).
  • 76
    • 78650126459 scopus 로고    scopus 로고
    • CCDC 784114 ((R,S)- 3 b) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via.
    • CCDC 784114 ((R,S)- 3 b) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.