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Volumn 45, Issue 3, 2006, Pages 481-485

Convenient and efficient Pd-catalyzed regioselective oxyfunctionalization of terminal olefins by using molecular oxygen as sole reoxidant

Author keywords

Acetoxylation; Alkenes; Oxygen; Palladium; Wacker oxidation

Indexed keywords

CATALYST ACTIVITY; KETONES; MOLECULAR STRUCTURE; OLEFINS; OXIDATION; OXYGEN;

EID: 30444437460     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200502886     Document Type: Article
Times cited : (218)

References (43)
  • 2
    • 0003678023 scopus 로고
    • Oxidations in Organic Chemistry
    • American Chemical Society, Washington, DC
    • b) M. Hudlucky, Oxidations in Organic Chemistry, American Chemical Society, Washington, DC, 1990 (ACS Monograph Series);
    • (1990) ACS Monograph Series
    • Hudlucky, M.1
  • 34
    • 30444433043 scopus 로고    scopus 로고
    • note
    • 2-DMSO system, which was effective for an intramolecular Wacker-type cyclization and acetoxylation, failed to promote the Wacker oxidation of 1-decene (< 1 % yield in 6 h).
  • 35
    • 30444454596 scopus 로고    scopus 로고
    • note
    • See the Supporting Information for the experimental details.
  • 38
    • 1042276609 scopus 로고    scopus 로고
    • There has been only one report of the selective synthesis of linear allylic acetates from terminal olefins: M. S. Chen, M. C. White, J. Am. Chem. Soc. 2004, 126, 1346; however, we confirmed that the acetoxylation of 1-eicosene hardly occurred with the above catalytic system.
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 1346
    • Chen, M.S.1    White, M.C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.