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Volumn 49, Issue 38, 2010, Pages 6877-6880

1,2,3-trisubstituted indanes by highly diastereoselective palladium-catalyzed oxyarylation of indenes with arylboronic acids and nitroxides

Author keywords

Homogeneous catalysis; Nitroxides; Palladium; Stereoselective reactions; Synthetic methods

Indexed keywords

ANTI ISOMERS; ARYLBORONIC ACIDS; DIASTEREOSELECTIVE; HOMOGENEOUS CATALYSIS; NITROXIDES; STEREOSELECTIVE REACTIONS; SYNTHETIC METHODS;

EID: 77956578134     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201002214     Document Type: Article
Times cited : (70)

References (51)
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    • The intramolecular oxidative carbofunctional ization of olefins has been far more intensively investigated than the intermolecular variants. For a review, see: J. P. Wolfe, Eur. J. Org. Chem. 2007, 571. Some recent publications:
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    • Kalyani, D.1    Sanford, M.S.2
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    • As a side product, the product of a double phenylation oxidation reaction was isolated in 9% yield (see the Supporting Information)
    • As a side product, the product of a double phenylation oxidation reaction was isolated in 9% yield (see the Supporting Information).
  • 51
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    • CCDC 771860 (3a) and CCDC 771861 (9) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • CCDC 771860 (3a) and CCDC 771861 (9) 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.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.