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Volumn 7, Issue 6, 2009, Pages 1226-1230

Preparation of 1-aryl-substituted isoindoline derivatives by sequential Morita-Baylis-Hillman and intramolecular Diels-Alder reactions

Author keywords

[No Author keywords available]

Indexed keywords

ALDIMINES; CYCLOADDUCTS; DIELS-ALDER CYCLOADDITIONS; INTRAMOLECULAR DIELS-ALDER REACTIONS; ISOINDOLINE; MORITA-BAYLIS-HILLMAN REACTIONS; NITRILE GROUPS; PROPARGYL;

EID: 62249140298     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b817954a     Document Type: Article
Times cited : (14)

References (61)
  • 10
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  • 13
    • 62249084601 scopus 로고    scopus 로고
    • PCT Int., WO 02046164
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  • 14
    • 27644490377 scopus 로고    scopus 로고
    • PCT Int., WO 00021950
    • C. N. Johnson and G. Stemp, PCT Int., WO 00021950, 2000, Chem. Abs., 132, 279110
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    • Johnson, C.N.1    Stemp, G.2
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    • 62249112717 scopus 로고    scopus 로고
    • PCT Int., WO 06025991
    • G. W. Muller, and H.-W. Man, PCT Int., WO 06025991, 2006, Chem. Abs., 144, 369911
    • (2006) Chem. Abs. , vol.144 , pp. 369911
    • Muller, G.W.1    Man, H.-W.2
  • 57
    • 37349106811 scopus 로고    scopus 로고
    • The use of Morita-Baylis-Hillman reactions to generate the dienophile component for subsequent intramolecular Diels-Alder cycloadditions has been employed in the syntheses of mniopetal F and sordarin analogues; see: -2998
    • K. N. Clary T. G. Back Synlett 2007 2995 2998
    • (2007) Synlett , pp. 2995
    • Clary, K.N.1    Back, T.G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.