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Volumn 8, Issue 12, 2006, Pages 2603-2606

Preparation of aliphatic ketones through a ruthenium-catalyzed tandem cross-metathesis/allylic alcohol isomerization

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EID: 33745556151     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol060918g     Document Type: Article
Times cited : (49)

References (46)
  • 15
    • 33644504470 scopus 로고    scopus 로고
    • For examples that include olefin metatheses, see: (f) Schmidt, B. Pure Appl. Chem. 2006, 78, 469.
    • (2006) Pure Appl. Chem. , vol.78 , pp. 469
    • Schmidt, B.1
  • 35
    • 0033564998 scopus 로고    scopus 로고
    • For studies on the decomposition of alkylidene 3, see: (a) Hoye, T. R.; Zhao, H. Org. Lett. 1999, 1, 169.
    • (1999) Org. Lett. , vol.1 , pp. 169
    • Hoye, T.R.1    Zhao, H.2
  • 40
    • 0001442835 scopus 로고    scopus 로고
    • For examples of ruthenium hydride formation through hydrogenation of ruthenium alkylidenes, see: (a) Caulton, K. G.; Olivan, M. Inorg. Chem. 1999, 38, 566.
    • (1999) Inorg. Chem. , vol.38 , pp. 566
    • Caulton, K.G.1    Olivan, M.2
  • 46
    • 33745554243 scopus 로고    scopus 로고
    • note
    • We anticipate that more functionalized allylic alcohols, if viable substrates in the cross metathesis step, will provide similar access to functionalized ketones through this tandem process.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.