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Volumn 48, Issue 39, 2009, Pages 7232-7235

Acid-catalyzed intramolecular [2+2] Cycloaddition of ene-allenones: Facile access to bicyclo[n.2.0] frameworks

Author keywords

Acid catalysis; Cycloaddition; Cyclobutanes; Multiple bonds; Used ring systems

Indexed keywords

[2 + 2] CYCLOADDITION; ACID CATALYSIS; CYCLOBUTANES; DIASTEREOSELECTIVITIES; FACILE ACCESS; MULTIPLE BONDS; TERTIARY CENTERS; USED-RING SYSTEMS;

EID: 70349922826     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200902471     Document Type: Article
Times cited : (45)

References (78)
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    • CCDC 739969 (37) and 739970 (6) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • CCDC 739969 (37) and 739970 (6) contain 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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    • Only the [2+2]-cycloaddition product 3 a was obtained when five equivalents of MeOH were added into the reaction mixture of la.
    • Only the [2+2]-cycloaddition product 3 a was obtained when five equivalents of MeOH were added into the reaction mixture of la.
    • , vol.22
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    • For more details, see the Supporting Information.
    • For more details, see the Supporting Information.
    • , vol.23


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.