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Volumn 65, Issue 6, 2000, Pages 1788-1792

Terminal alkyne-ethylene cross-metathesis: Reaction of 1-substituted propargyl esters at elevated ethylene pressure

Author keywords

[No Author keywords available]

Indexed keywords

1,3 BUTADIENE DERIVATIVE; ALKYNE; ESTER; ETHYLENE;

EID: 0034708557     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo9916941     Document Type: Article
Times cited : (87)

References (30)
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    • 0033516679 scopus 로고    scopus 로고
    • The substituted alkyne requires longer reaction times (50 h) at 1 atm of ethylene to obtain 87% conversion and 73% isolated yield; see: Kinoshita, A.; Sakakibara, N.; Mori, M. Tetrahedron 1999, 55, 8155.
    • (1999) Tetrahedron , vol.55 , pp. 8155
    • Kinoshita, A.1    Sakakibara, N.2    Mori, M.3
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    • note
    • 1H NMR.
  • 21
    • 0343415092 scopus 로고    scopus 로고
    • note
    • The reaction conducted at 1 atm continued to convert to product 3 even after 50 h, but only reached 68% 3 after 95 h. The data taken after ca. 50 h are not considered reliable since evaporative loss of solvent became significant at 1 atm of pressure (balloon). Evaporative loss of solvent was not serious at higher pressures or shorter reaction times.
  • 26
    • 0011391877 scopus 로고
    • Use of related lipases: (a) Viola, A.; Duddling, G. F.; Proverb, R. J. J. Am. Chem. Soc. 1977, 99, 7390. (b) Kuenstler, T.; Schollmeyer, D.; Singer, H.; Steigerwald, M. Tetrahedron: Asymmetry 1993, 4, 1645. (c) Glaenzer, B. I.; Faber, K.; Griengl, H. Tetrahedron 1987, 43, 5791. (d) Waldinger, C.; Schneider, M.; Botta, M.; Corelli, F.; Summa, V. Tetrahedron: Asymmetry 1996, 7, 1485. (e) Enantioselectivity model: Burgess, K. B.; Jennings, L. D. J. Am. Chem. Soc. 1991, 113, 6129.
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    • 0027170601 scopus 로고
    • Use of related lipases: (a) Viola, A.; Duddling, G. F.; Proverb, R. J. J. Am. Chem. Soc. 1977, 99, 7390. (b) Kuenstler, T.; Schollmeyer, D.; Singer, H.; Steigerwald, M. Tetrahedron: Asymmetry 1993, 4, 1645. (c) Glaenzer, B. I.; Faber, K.; Griengl, H. Tetrahedron 1987, 43, 5791. (d) Waldinger, C.; Schneider, M.; Botta, M.; Corelli, F.; Summa, V. Tetrahedron: Asymmetry 1996, 7, 1485. (e) Enantioselectivity model: Burgess, K. B.; Jennings, L. D. J. Am. Chem. Soc. 1991, 113, 6129.
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    • 0001478678 scopus 로고
    • Use of related lipases: (a) Viola, A.; Duddling, G. F.; Proverb, R. J. J. Am. Chem. Soc. 1977, 99, 7390. (b) Kuenstler, T.; Schollmeyer, D.; Singer, H.; Steigerwald, M. Tetrahedron: Asymmetry 1993, 4, 1645. (c) Glaenzer, B. I.; Faber, K.; Griengl, H. Tetrahedron 1987, 43, 5791. (d) Waldinger, C.; Schneider, M.; Botta, M.; Corelli, F.; Summa, V. Tetrahedron: Asymmetry 1996, 7, 1485. (e) Enantioselectivity model: Burgess, K. B.; Jennings, L. D. J. Am. Chem. Soc. 1991, 113, 6129.
    • (1987) Tetrahedron , vol.43 , pp. 5791
    • Glaenzer, B.I.1    Faber, K.2    Griengl, H.3
  • 29
    • 0030000285 scopus 로고    scopus 로고
    • Use of related lipases: (a) Viola, A.; Duddling, G. F.; Proverb, R. J. J. Am. Chem. Soc. 1977, 99, 7390. (b) Kuenstler, T.; Schollmeyer, D.; Singer, H.; Steigerwald, M. Tetrahedron: Asymmetry 1993, 4, 1645. (c) Glaenzer, B. I.; Faber, K.; Griengl, H. Tetrahedron 1987, 43, 5791. (d) Waldinger, C.; Schneider, M.; Botta, M.; Corelli, F.; Summa, V. Tetrahedron: Asymmetry 1996, 7, 1485. (e) Enantioselectivity model: Burgess, K. B.; Jennings, L. D. J. Am. Chem. Soc. 1991, 113, 6129.
    • (1996) Tetrahedron: Asymmetry , vol.7 , pp. 1485
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  • 30
    • 0001364513 scopus 로고
    • Use of related lipases: (a) Viola, A.; Duddling, G. F.; Proverb, R. J. J. Am. Chem. Soc. 1977, 99, 7390. (b) Kuenstler, T.; Schollmeyer, D.; Singer, H.; Steigerwald, M. Tetrahedron: Asymmetry 1993, 4, 1645. (c) Glaenzer, B. I.; Faber, K.; Griengl, H. Tetrahedron 1987, 43, 5791. (d) Waldinger, C.; Schneider, M.; Botta, M.; Corelli, F.; Summa, V. Tetrahedron: Asymmetry 1996, 7, 1485. (e) Enantioselectivity model: Burgess, K. B.; Jennings, L. D. J. Am. Chem. Soc. 1991, 113, 6129.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 6129
    • Burgess, K.B.1    Jennings, L.D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.