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Volumn 31, Issue 19, 2012, Pages 6843-6850

Mechanistic studies of azaphilic versus carbophilic activation by gold(I) in the gold/palladium dual-catalyzed rearrangement of alkenyl vinyl aziridines

Author keywords

[No Author keywords available]

Indexed keywords

ALKENYL; AZIRIDINES; COCATALYST; GOLD CATALYSIS; GOLD/PALLADIUM; LEWIS ACID; LEWIS-ACID ACTIVATION; MECHANISTIC STUDIES;

EID: 84867386033     PISSN: 02767333     EISSN: 15206041     Source Type: Journal    
DOI: 10.1021/om300671j     Document Type: Article
Times cited : (69)

References (78)
  • 25
    • 84867354379 scopus 로고    scopus 로고
    • Reference 22.
    • Reference 22.
  • 53
    • 77950851953 scopus 로고    scopus 로고
    • As evidenced by its resistance to protonolysis. See: Roth, K. E.; Blum, S. A. Organometallics 2010, 29, 1712
    • (2010) Organometallics , vol.29 , pp. 1712
    • Roth, K.E.1    Blum, S.A.2
  • 76
    • 0037652138 scopus 로고    scopus 로고
    • The data presently available are also consistent with a syn addition of the Lewis acid/amide σ-bond of 14 across the tethered olefin followed by transmetalation to the Pd π-allyl cation, but we suspect the trapping of the Pd electrophile may be a much faster pathway. For one related example of syn addition of Li- and Na-amides across olefins, see: Ates, A.; Quinet, C. Eur. J. Org. Chem. 2003, 1623
    • (2003) Eur. J. Org. Chem. , pp. 1623
    • Ates, A.1    Quinet, C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.