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Volumn , Issue 17, 2007, Pages 2844-2849

Allene substitution-controlled switching of dimerization to cycloisomerization in the PdII-catalyzed reaction of terminal α-allenones

Author keywords

Allenes; Cyclization; Heterocycles; Palladium; Substituent effects

Indexed keywords


EID: 34250796820     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.200700128     Document Type: Article
Times cited : (49)

References (44)
  • 1
    • 33746294594 scopus 로고    scopus 로고
    • For selected reviews, see: a, Eds, G. W. Gribble, J. A. Joule, Elsevier: Oxford
    • For selected reviews, see: a) X.-L. Hou, Z. Yang, K.-S. Yeung, H. N. C. Wong, in Progress in Heterocyclic Chemistry (Eds.: G. W. Gribble, J. A. Joule), Elsevier: Oxford, 2005, vol. 17, pp. 142-171;
    • (2005) Progress in Heterocyclic Chemistry , vol.17 , pp. 142-171
    • Hou, X.-L.1    Yang, Z.2    Yeung, K.-S.3    Wong, H.N.C.4
  • 3
    • 0001176061 scopus 로고    scopus 로고
    • Eds, A. R. Katritzky, C. W. Rees, E. F. V. Scriven, Elsevier, Oxford
    • c) B. A. Keay, P. W. Dibble in Comprehensive Heterocyclic Chemistry II, vol. 2 (Eds.: A. R. Katritzky, C. W. Rees, E. F. V. Scriven), Elsevier, Oxford, 1997, pp. 395-436;
    • (1997) Comprehensive Heterocyclic Chemistry II , vol.2 , pp. 395-436
    • Keay, B.A.1    Dibble, P.W.2
  • 10
    • 22944485617 scopus 로고    scopus 로고
    • For reviews, see: a
    • For reviews, see: a) S. Ma, Chem. Rev. 2005, 105, 2829;
    • (2005) Chem. Rev , vol.105 , pp. 2829
    • Ma, S.1
  • 11
    • 4544320494 scopus 로고    scopus 로고
    • N. Krause, A. S. K. Hashmi, Wiley-VCH, Weinheim
    • b) Modern Allene Chemistry, N. Krause, A. S. K. Hashmi, Wiley-VCH, Weinheim, 2004;
    • (2004) Modern Allene Chemistry
  • 16
    • 34250883692 scopus 로고    scopus 로고
    • Angew. Chem. 2000, 112, 3737;
    • (2000) Chem , vol.112 , pp. 3737
    • Angew1
  • 22
    • 0037664955 scopus 로고    scopus 로고
    • A. S. K. Hashmi, Wiley-VCH, Weinheim
    • b) Organic Synthesis Highlights V, A. S. K. Hashmi, Wiley-VCH, Weinheim, 2003, pp. 56-67;
    • (2003) Organic Synthesis Highlights V , pp. 56-67
  • 30
    • 34250869344 scopus 로고    scopus 로고
    • Angew. Chem. 2000, 112, 2382.
    • (2000) Chem , vol.112 , pp. 2382
    • Angew1
  • 34
    • 34250842999 scopus 로고    scopus 로고
    • Angew. Chem. 2006, 118, 4613;
    • (2006) Chem , vol.118 , pp. 4613
    • Angew1
  • 43
    • 0035900403 scopus 로고    scopus 로고
    • α-allenol (-)-2c has been previously prepared as a mixture of regio- and diastereoisomers using stannane chemistry: d) A. McCluskey, I. W. Muderawan, Muntari, D. J. Young, J. Org. Chem. 2001, 66, 7811.
    • α-allenol (-)-2c has been previously prepared as a mixture of regio- and diastereoisomers using stannane chemistry: d) A. McCluskey, I. W. Muderawan, Muntari, D. J. Young, J. Org. Chem. 2001, 66, 7811.
  • 44
    • 34250831924 scopus 로고    scopus 로고
    • Full spectroscopic and analytical data for compounds not included in this Experimental Section are described in the Supporting Information. It contains compound characterization data and experimental procedures for compounds 2a-d, )-2f, 3a-h, )-3k, )-31, 4a-g, -4j, 5a-j, and 5m-o
    • Full spectroscopic and analytical data for compounds not included in this Experimental Section are described in the Supporting Information. It contains compound characterization data and experimental procedures for compounds 2a-d, (+)-2f, 3a-h, (+)-3k, (+)-31, 4a-g, (+)-4j, 5a-j, and 5m-o.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.