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Volumn 51, Issue 48, 2010, Pages 6349-6352

Domino reaction of arylaldehydes and 1-acetylcyclopropanecarboxamides: One-pot access to highly functionalized spiropiperidine-2,4-diones

Author keywords

Ketoamides; Arylaldehydes; Domino reaction; Michael addition; Piperidine 2,4 diones

Indexed keywords

1 ACETYLCYCLOPROPANECARBOXAMIDE; ALDEHYDE DERIVATIVE; AMIDE; PIPERIDINE DERIVATIVE; SPIROPIPERIDINE 2,4 DIONE; UNCLASSIFIED DRUG;

EID: 78049409621     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2010.09.133     Document Type: Article
Times cited : (15)

References (51)
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    • note
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    • Spirocyclopropanes are present in a number of pharmacologically interesting natural products, such as the cytotoxic illudins. For selected papers see: M.C. Pirrung, and H. Liu Org. Lett. 5 2003 1983
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    • CCDC 771686 (3a) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • CCDC 771686 (3a) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
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    • note
    • 4: C, 78.33; H, 5.88; N, 4.81; found: C, 78.30; H, 5.89; N, 4.79.
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    • For synthetic details, see Supplementary data
    • For synthetic details, see Supplementary data.
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    • The yields corresponding to products 3 could not be further improved after several trials
    • The yields corresponding to products 3 could not be further improved after several trials.
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    • It was observed in our experimental that even though excessive arylaldehyde was introduced to the reaction system, there is a strong tendency for the formation of compounds 3
    • It was observed in our experimental that even though excessive arylaldehyde was introduced to the reaction system, there is a strong tendency for the formation of compounds 3.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.