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Volumn 45, Issue 45, 2006, Pages 7618-7622

A second-generation catalyst for intermolecular hydroacylation of alkenes and alkynes using β-S-substituted aldehydes: The role of a hemilabile P-O-P ligand

Author keywords

C H activation; Hemilabile ligands; Homogeneous catalysis; Intermolecular hydroacylation; Rhodium

Indexed keywords

ACTIVATION ANALYSIS; ACYLATION; CATALYST ACTIVITY; MOLECULAR STRUCTURE; OLEFINS; OXYGEN; RHODIUM; SUBSTITUTION REACTIONS;

EID: 33845204295     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200603133     Document Type: Article
Times cited : (139)

References (42)
  • 23
    • 33845233052 scopus 로고    scopus 로고
    • note
    • 2 (Ref. [4a]) can be isolated, it is relatively air sensitive, and in our hands its use led to variable results.
  • 33
    • 33845231034 scopus 로고    scopus 로고
    • note
    • 4) was also active, although the reaction required 4 h to reach completion.
  • 34
    • 33845201872 scopus 로고    scopus 로고
    • note
    • The product from entry 4 (Table 2) was obtained in 33 % yield with the original catalyst. See Ref. [7a].
  • 42
    • 37049091603 scopus 로고
    • For an example of a spectroscopically characterized acyl-hydrido species that undergoes intramolecular hydroacylation, see: D. Milstein, J. Chem. Soc. Chem. Commun. 1982, 1357.
    • (1982) J. Chem. Soc. Chem. Commun. , pp. 1357
    • Milstein, D.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.