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Volumn 48, Issue 48, 2009, Pages 9139-9142

Enantioselective palladium-catalyzed direct arylations at ambient temperature: access to indanes with quaternary stereocenters

Author keywords

Asymmetric catalysis; C h activation; Direct arylation; Palladium; Stereocenters

Indexed keywords

AMBIENT TEMPERATURES; ARYLATIONS; ASYMMETRIC CATALYSIS; C-H ACTIVATION; DIMETHYLACETAMIDE; DIRECT ARYLATION; ENANTIOMERIC EXCESS; ENANTIOSELECTIVE; PHOSPHORAMIDITE LIGANDS; QUATERNARY STEREOCENTERS; REACTION CONDITIONS; STEREOCENTERS; STEREOGENIC CENTERS;

EID: 70449575808     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200905060     Document Type: Article
Times cited : (166)

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    • In general, electron-poor substrates react faster, which is in agreement with the described mechanism of reference [8].
    • In general, electron-poor substrates react faster, which is in agreement with the described mechanism of reference [8].
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    • See the Supporting Information. CCDC 745459 (5j) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • See the Supporting Information. CCDC 745459 (5j) 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.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.