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Volumn 15, Issue 8, 2013, Pages 1938-1941

Erratum: Alder-ene reactions of arynes (Org. Lett. (2013) 15:8 (1938-1941) DOI:10.1021/ol4005905);Alder-ene reactions of arynes

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EID: 84876557127     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol500038u     Document Type: Erratum
Times cited : (82)

References (43)
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    • In; Akermann, L. Wiley-VCH: Weinheim, Germany
    • Chen, Y.; Larock, R. C. In Modern Arylation Methods; Akermann, L., Ed.; Wiley-VCH: Weinheim, Germany, 2009; pp 401-473.
    • (2009) Modern Arylation Methods , pp. 401-473
    • Chen, Y.1    Larock, R.C.2
  • 11
    • 84876562522 scopus 로고    scopus 로고
    • Abstracts of Papers; 244th American Chemical Society Meeting, Philadelphia, PA; Washington, DC, ORGN 355
    • Wang, K.-P.; Yun, S. Y.; Lee, D. Abstracts of Papers; 244th American Chemical Society Meeting, Philadelphia, PA; Washington, DC, 2012, ORGN 355.
    • (2012)
    • Wang, K.-P.1    Yun, S.Y.2    Lee, D.3
  • 40
    • 47249130867 scopus 로고    scopus 로고
    • For a review on dehydro Diels-Alder reaction, see: Wessig, P.; Müller, G. Chem. Rev. 2008, 108, 2051
    • (2008) Chem. Rev. , vol.108 , pp. 2051
    • Wessig, P.1    Müller, G.2
  • 41
    • 20044390256 scopus 로고    scopus 로고
    • Review on the gem -dialkyl effect
    • Review on the gem -dialkyl effect: Jung, M. E.; Piizzi, G. Chem. Rev. 2005, 105, 1735
    • (2005) Chem. Rev. , vol.105 , pp. 1735
    • Jung, M.E.1    Piizzi, G.2
  • 42
    • 84863534825 scopus 로고    scopus 로고
    • During the hydrovinylative cyclization of bis-1,3-diynes, it was noticed that different heteroatoms in the tether confer profound impact on their reactivity, see: Under these reaction conditions, NTs-containing bis-1,3-diynes did not readily participate in the hydrovinylative cyclization; instead they underwent hexadehydro Diels-Alder reaction to form arynes. An account of the aryne formation and their trapping with halogenated hydrocarbons will be described elsewhere
    • During the hydrovinylative cyclization of bis-1,3-diynes, it was noticed that different heteroatoms in the tether confer profound impact on their reactivity, see: Yun, S. Y.; Wang, K.-P.; Kim, M.; Lee, D. J. Am. Chem. Soc. 2012, 134, 10783 Under these reaction conditions, NTs-containing bis-1,3-diynes did not readily participate in the hydrovinylative cyclization; instead they underwent hexadehydro Diels-Alder reaction to form arynes. An account of the aryne formation and their trapping with halogenated hydrocarbons will be described elsewhere
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 10783
    • Yun, S.Y.1    Wang, K.-P.2    Kim, M.3    Lee, D.4


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