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Volumn 68, Issue 4, 2003, Pages 1601-1602

Iridium-catalyzed oppenauer oxidations of primary alcohols using acetone or 2-butanone as oxidant

Author keywords

[No Author keywords available]

Indexed keywords

BIFUNCTIONAL CATALYSTS;

EID: 0037458962     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0262560     Document Type: Article
Times cited : (88)

References (19)
  • 10
    • 0003025653 scopus 로고
    • Although a detailed mechanism has not yet been determined, it seems possible that the dimeric ester 3 was formed via the corresponding hemiacetal intermediate. The reaction of bromobenzaldehyde (2f) in the presence of the Ir catalyst 4 (2f:4 = 100:1 mole ratio) gave a trace amount of 3f under reflux for 16 h, indicating that the contribution of the mechanism via the acylhydridometal complex is negligible. For the mechanism via the acylhydridometal complex, see: Horino, H.; Ito, T.; Yamamoto, A. Chem. Lett. 1978, 17-20.
    • (1978) Chem. Lett. , pp. 17-20
    • Horino, H.1    Ito, T.2    Yamamoto, A.3
  • 16
    • 0001434584 scopus 로고    scopus 로고
    • 2: Dobler, C.; Mehltretter, G. M.; Sundermeier, U.; Eckert, M.; Militzer, H.-C.; Beller, M. Tetrahedron Lett. 2001, 42, 8447-8449.
    • (1998) J. Org. Chem. , vol.63 , pp. 3185-3189
    • Peterson, K.P.1    Larock, R.C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.