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Volumn 51, Issue 16, 2012, Pages 3766-3778

Arynes and cyclohexyne in natural product synthesis

Author keywords

arynes; cyclohexyne; indolynes; natural products; total synthesis

Indexed keywords

ARYNES; CYCLOHEXYNE; INDOLYNES; NATURAL PRODUCTS; TOTAL SYNTHESIS;

EID: 84859765100     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201107485     Document Type: Review
Times cited : (460)

References (116)
  • 2
    • 84891029339 scopus 로고    scopus 로고
    • For a monograph, see (Eds.: F. Diederich, P. J. Stang, R. R. Tykwinski), Wiley-VCH, Weinheim
    • For a monograph, see Acetylene Chemistry, Chemistry, Biology, and Material Science (Eds.:, F. Diederich, P. J. Stang, R. R. Tykwinski,), Wiley-VCH, Weinheim, 2005.
    • (2005) Acetylene Chemistry, Chemistry, Biology, and Material Science
  • 3
    • 84982075527 scopus 로고
    • "Es ist bisher noch kein Kohlenstoffring, der eine derifache Bindung enthalten würde, bekannt geworden.", L. Ruzicka, M. Hürbin, H. A. Boekenoogen, Helv. Chim. Acta 1933, 16, 498-505.
    • (1933) Helv. Chim. Acta , vol.16 , pp. 498-505
    • Ruzicka, L.1    Hürbin, M.2    Boekenoogen, H.A.3
  • 5
    • 0002073050 scopus 로고
    • (Eds.: P. J. Stang, F. Diederich), VCH, Weinheim
    • R. Gleiter, R. Merger, in Modern Acetylene Chemistry (Eds.:, P. J. Stang, F. Diederich,), VCH, Weinheim, 1995, pp. 285-319
    • (1995) Modern Acetylene Chemistry , pp. 285-319
    • Gleiter, R.1    Merger, R.2
  • 7
    • 79960322536 scopus 로고    scopus 로고
    • (Ed.: H. Dodziuk), Wiley-VCH, Weinheim
    • H. Hopf, J. Grunenberg, in Strained Hydrocarbons (Ed.:, H. Dodziuk,), Wiley-VCH, Weinheim, 2009, pp. 375-398; for reviews, see
    • (2009) Strained Hydrocarbons , pp. 375-398
    • Hopf, H.1    Grunenberg, J.2
  • 16
    • 33748217248 scopus 로고
    • for reviews, see
    • Angew. Chem. Int. Ed. Engl. 1995, 34, 1721-1723; for reviews, see
    • (1995) Angew. Chem. Int. Ed. Engl. , vol.34 , pp. 1721-1723
  • 34
    • 0000264238 scopus 로고
    • (Eds.: B. M. Trost, I. Fleming), Pergamon, New York
    • S. V. Kessar, in Comprehensive Organic Synthesis, Vol. 4 (Eds.:, B. M. Trost, I. Fleming,), Pergamon, New York, 1991, pp. 483-515
    • (1991) Comprehensive Organic Synthesis, Vol. 4 , pp. 483-515
    • Kessar, S.V.1
  • 48
  • 50
    • 84859775214 scopus 로고    scopus 로고
    • Throughout the text the term "[X+Y] cycloaddition" does not imply a concerted reaction mechanism, but is used to define the number of atoms X and Y that react to give a cyclic product
    • Throughout the text the term "[X+Y] cycloaddition" does not imply a concerted reaction mechanism, but is used to define the number of atoms X and Y that react to give a cyclic product.
  • 69
  • 75
    • 33745031170 scopus 로고    scopus 로고
    • This only holds true if both regioisomers react by the same reaction pathway, that is, both via aryne or both via organometal species, and a change in the substitution pattern does not lead to a change in reaction mechanism; see Ref. [30d] and
    • This only holds true if both regioisomers react by the same reaction pathway, that is, both via aryne or both via organometal species, and a change in the substitution pattern does not lead to a change in reaction mechanism; see Ref. [30d] and, E. Guitián, D. Pérez, D. Peña, Top. Organomet. Chem. 2005, 14, 109-147.
    • (2005) Top. Organomet. Chem. , vol.14 , pp. 109-147
    • Guitián, E.1    Pérez, D.2    Peña, D.3
  • 77
  • 111
  • 113
    • 77953115779 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2010, 49, 4092-4095.
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 4092-4095
  • 115
    • 79952634328 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2011, 50, 2962-2965.
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 2962-2965


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.