메뉴 건너뛰기




Volumn , Issue 1, 2000, Pages 217-224

Mechanisms of cyclopalladation reactions in acetic acid: Not so simple one-pot processes

Author keywords

Acetic acid; Cyclopalladation; Palladium; Pd C bond stability; Polynuclear species; Reaction mechanisms

Indexed keywords

ACETIC ACID; ACTIVATION ANALYSIS; CHEMICAL ACTIVATION; COORDINATION REACTIONS; DIMERS; KINETICS; ORGANOMETALLICS; PALLADIUM COMPOUNDS; PH;

EID: 0033985884     PISSN: 14341948     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1099-0682(200001)2000:1<217::AID-EJIC217>3.0.CO;2-Q     Document Type: Article
Times cited : (51)

References (40)
  • 39
    • 85153260598 scopus 로고    scopus 로고
    • note
    • 2] in acetic acid for 3 h at 70 °C produces mainly mono-cyclometallated acetato dimer plus free imine.
  • 40
    • 85153258976 scopus 로고    scopus 로고
    • note
    • The direct condensation of e plus p-clorobenzaldehyde in acetic acid yields quantitatively imine a. In addition, after 3 hours in refluxing acetic acid only a 3% of decomposition of imine a is observed as monitored by GC chromatography.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.