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Volumn 19, Issue 8, 2008, Pages 998-1004

Experimental and theoretical studies on the asymmetric cyanosilylation of C2-symmetric hydrazones

Author keywords

[No Author keywords available]

Indexed keywords

1 [(2 METHYLL)PROPYLIDENEAMINE] 2,5 DIPHENYLPYRROLIDINE; 1 [(3 PHENYL)PROPYLIDENEAMINE] 2,5 DIPHENYLPYRROLIDINE; 1 AMINO 2,5 DIPHENYLPYRROLIDINE; 1 HEXYLIDENEAMINE 2,5 DIPHENYLPYRROLIDINE; HYDRAZONE DERIVATIVE; NITRILE; NITROGEN; PHENYL GROUP; PYRROLIDINE DERIVATIVE; TRIMETHYLSILYL CYANIDE; TRIMETHYLSILYL DERIVATIVE;

EID: 43149083026     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2008.03.020     Document Type: Article
Times cited : (15)

References (59)
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    • note
    • In full analogy with enamines, the nucleophilic character of the azomethine carbon of hydrazones demands an effective conjugation between the amino nitrogen and the CN double bond. Consequently, the electrophilic, imine-like reactivity of hydrazones requires the loss of the conjugation and, hence, conformations clearly deviated from planarity. Muñoz, J. M. Ph. D. Thesis, University of Seville, 2006.
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    • note
    • Full crystallographic data for these structures have been deposited with the Cambridge Crystallographic Data Centre as supplementary publications CCDC 679390 and 679391. These data can be obtained free of charge on application to CCDC, 12, Union Road, Cambridge CB2 1EZ, UK; fax: +44 (1223)336033; or e-mail: deposit@ccdc.cam.ac.uk.
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    • note
    • 2AlCl/C(2′) repulsive interaction.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.