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Volumn 20, Issue 35, 2014, Pages 11084-11090

Synthesis of 1-indanols and 1-indanamines by intramolecular palladium(0)-catalyzed C(sp3)-H arylation: Impact of conformational effects

Author keywords

C C coupling; C H activation; conformation analysis; palladium

Indexed keywords

ACTIVATION ANALYSIS; AROMATIC COMPOUNDS; CATALYSIS; CONFORMATIONS;

EID: 84906787434     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201402907     Document Type: Article
Times cited : (31)

References (61)
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    • 0-catalyzed intramolecular C-H arylation of cyclopropanes, see
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    • For a seminal example in C-H insertion chemistry, see.
    • For a seminal example in C-H insertion chemistry, see:, H. M. L. Davies, P. Ren, J. Am. Chem. Soc. 2001, 123, 2070.
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    • For selected examples, see
    • For selected examples, see
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    • CCDC-986266 (2 t), 986267 (A1), and 990781 (A2) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via.
    • CCDC-986266 (2 t), 986267 (A1), and 990781 (A2) 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.
  • 57
    • 84906786526 scopus 로고    scopus 로고
    • These low-to-moderate yields are mainly attributed to the formation of insoluble material during the reaction. The protodebrominated product was the only observed soluble compound in the reaction of 1 t. In addition, an independently prepared cis/trans diastereoisomeric mixture of 2 t was stable under the reaction conditions, with no change in the diastereomeric ratio.
    • These low-to-moderate yields are mainly attributed to the formation of insoluble material during the reaction. The protodebrominated product was the only observed soluble compound in the reaction of 1 t. In addition, an independently prepared cis/trans diastereoisomeric mixture of 2 t was stable under the reaction conditions, with no change in the diastereomeric ratio.
  • 60
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    • [2c,d, 18] respectively, through DFT calculations.
    • [2c,d, 18] respectively, through DFT calculations.
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    • For a study on the effect of the base and ligand on the CMD mechanism, see.
    • For a study on the effect of the base and ligand on the CMD mechanism, see:, C. E. Kefalidis, O. Baudoin, E. Clot, Dalton Trans. 2010, 39, 10528.
    • (2010) Dalton Trans. , vol.39 , pp. 10528
    • Kefalidis, C.E.1    Baudoin, O.2    Clot, E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.