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Volumn 129, Issue 8, 2007, Pages 2230-2231

Synthesis of acyclic α,β-unsaturated ketones via Pd(II)-catalyzed intermolecular reaction of alkynamides and alkenes

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE DERIVATIVE; AMIDE; KETONE DERIVATIVE; PALLADIUM;

EID: 33847654631     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja068886f     Document Type: Article
Times cited : (34)

References (32)
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    • (d) Thiel, O. R. In Transition Metals for Organic Synthesis; Beller, M., Bolm, C., Eds.; Wiley-VCH: Weinheim, Germany, 2004, Vol. 1 pp 321-333.
    • (2004) Transition Metals for Organic Synthesis , vol.1 , pp. 321-333
    • Thiel, O.R.1
  • 10
    • 33644933443 scopus 로고    scopus 로고
    • For recent representative examples of oxidative coupling reactions catalyzed by Pd(II) see (a) Yip, K.-T.; Yang, M.; Law, K.-L.; Zhu, N.-Y.; Yang, D. J. Am. Chem. Soc. 2006, 128, 3130-3131.
    • For recent representative examples of oxidative coupling reactions catalyzed by Pd(II) see (a) Yip, K.-T.; Yang, M.; Law, K.-L.; Zhu, N.-Y.; Yang, D. J. Am. Chem. Soc. 2006, 128, 3130-3131.
  • 15
    • 33746494993 scopus 로고    scopus 로고
    • For representative examples of α,β-unsaturated ketone synthesis via oxidative reaction catalyzed by Pd(II) see (a) Ito, Y.; Hirao, T.; Saegusa, T. J. Org. Chem. 1978, 43, 1011-1013.
    • For representative examples of α,β-unsaturated ketone synthesis via oxidative reaction catalyzed by Pd(II) see (a) Ito, Y.; Hirao, T.; Saegusa, T. J. Org. Chem. 1978, 43, 1011-1013.
  • 19
    • 33847686576 scopus 로고    scopus 로고
    • Reference guide provided by Bruker, published in 1994.
    • (b) Reference guide provided by Bruker, published in 1994.
  • 20
    • 33847618578 scopus 로고    scopus 로고
    • A Pd-alkynl intermediate may be considered as another possibility; we disfavor such an intermediate as a major contributor to product formation, however, because it is inconsistent with the requirement for a pentynamide or hexynamide backbone
    • A Pd-alkynl intermediate may be considered as another possibility; we disfavor such an intermediate as a major contributor to product formation, however, because it is inconsistent with the requirement for a pentynamide or hexynamide backbone.
  • 21
    • 0034838172 scopus 로고    scopus 로고
    • For a representative example and additional references see
    • For a representative example and additional references see Littke, A. F.; Fu, G. C. J. Am. Chem. Soc. 2001, 123, 6989-7000.
    • (2001) J. Am. Chem. Soc , vol.123 , pp. 6989-7000
    • Littke, A.F.1    Fu, G.C.2
  • 22
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    • For representative reviews of the Wacker oxidation see a
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    • (1962) Chem. Ind , pp. 54-62
    • Smidt, J.1
  • 23
    • 85083243520 scopus 로고
    • (b) Tsuji, J. Synthesis 1984, 5, 369-384.
    • (1984) Synthesis , vol.5 , pp. 369-384
    • Tsuji, J.1
  • 26
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    • For reviews of the Heck reaction see a
    • For reviews of the Heck reaction see (a) Heck, R. F. Org. React. 1982, 27, 345-390.
    • (1982) Org. React , vol.27 , pp. 345-390
    • Heck, R.F.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.