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Volumn 73, Issue 14, 2008, Pages 5651-5653

Straightforward synthesis of α,β-unsaturated thioesters via ruthenium-catalyzed olefin cross-metathesis with thioacrylate

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL REACTIONS; RUTHENIUM;

EID: 48249088445     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo800879e     Document Type: Article
Times cited : (31)

References (48)
  • 5
    • 0004155427 scopus 로고
    • 4th ed, Freeman: New York
    • (b) Stryer, L. Biochemistry, 4th ed.; Freeman: New York, 1995.
    • (1995) Biochemistry
    • Stryer, L.1
  • 17
    • 33646447726 scopus 로고    scopus 로고
    • For a review on thioester chemistry developed in the last 10 years, see
    • For a review on thioester chemistry developed in the last 10 years, see: Fujiwara, S.-I.; Kambe, N. Top. Curr. Chem. 2005, 251, 87-140.
    • (2005) Top. Curr. Chem , vol.251 , pp. 87-140
    • Fujiwara, S.-I.1    Kambe, N.2
  • 28
    • 48249097700 scopus 로고    scopus 로고
    • The classical synthetic methods are described in the Supporting Information of ref 9b.
    • The classical synthetic methods are described in the Supporting Information of ref 9b.
  • 31
  • 42
  • 45
    • 48249109362 scopus 로고    scopus 로고
    • See the Supporting Information
    • See the Supporting Information.
  • 48
    • 48249135329 scopus 로고    scopus 로고
    • Cross-metathesis with 3,3-dimethyl-1-butene was attempted but product formation was not observed. The reaction was performed under the regular conditions (as specified in Table 2), although with 3,3-dimethyl-1-butene as cosolvent.
    • Cross-metathesis with 3,3-dimethyl-1-butene was attempted but product formation was not observed. The reaction was performed under the regular conditions (as specified in Table 2), although with 3,3-dimethyl-1-butene as cosolvent.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.