Synthesis 2013; 45(15): 2088-2092
DOI: 10.1055/s-0033-1338471
special topic
© Georg Thieme Verlag Stuttgart · New York

Rhodium-Catalyzed Dimerization of Arylacetylenes and Addition of Malonates­ to 1,3-Enynes

Katsufumi Mochizuki
Department of Chemistry, Faculty of Science and Technology, Keio University, 3-14-1 Hiyoshi, Kohoku-ku, Yokohama, Kanagawa 223-8522, Japan   Fax: +81(45)5661591   eMail: kakiuchi@chem.keio.ac.jp
,
Kazunori Sakai
Department of Chemistry, Faculty of Science and Technology, Keio University, 3-14-1 Hiyoshi, Kohoku-ku, Yokohama, Kanagawa 223-8522, Japan   Fax: +81(45)5661591   eMail: kakiuchi@chem.keio.ac.jp
,
Takuya Kochi
Department of Chemistry, Faculty of Science and Technology, Keio University, 3-14-1 Hiyoshi, Kohoku-ku, Yokohama, Kanagawa 223-8522, Japan   Fax: +81(45)5661591   eMail: kakiuchi@chem.keio.ac.jp
,
Fumitoshi Kakiuchi*
Department of Chemistry, Faculty of Science and Technology, Keio University, 3-14-1 Hiyoshi, Kohoku-ku, Yokohama, Kanagawa 223-8522, Japan   Fax: +81(45)5661591   eMail: kakiuchi@chem.keio.ac.jp
› Institutsangaben
Weitere Informationen

Publikationsverlauf

Received: 22. Februar 2013

Accepted after revision: 02. April 2013

Publikationsdatum:
08. Mai 2013 (online)


Abstract

An 8-quinolinolato rhodium catalyst was found to be effective for head-to-tail selective dimerization of arylacetylenes. Formation of substituted cyclopentene and allene derivatives via alkyne dimerization and subsequent addition of malonates was also catalyzed by the 8-quinolinolato rhodium catalyst in the presence of cesium fluoride. One-pot reaction using palladium-catalyzed alkyne dimerization in conjunction with rhodium-catalyzed addition of malonates was also possible.

Supporting Information

 
  • References

  • 1 Modern Acetylene Chemistry . Stang PJ, Diederich F. VCH; Weinheim: 1995
  • 2 Trost BM. Science 1991; 254: 1471

    • For reviews, see:
    • 3a Bustelo E, Dixneuf PH In Handbook of C–H Transformations: Applications in Organic Synthesis . Vol. 1. Dyker G. Wiley-VCH; Weinheim: 2005: 62-72
    • 3b Ritleng V, Sirlin C, Pfeffer M. Chem. Rev. 2002; 102: 1731

      For examples of E-selective head-to-head dimerization, see:
    • 4a Ogoshi S, Ueta M, Oka M.-a, Kurosawa H. Chem. Commun. 2004; 2732
    • 4b Ciclosi M, Estevan F, Lahuerta P, Passarelli V, Pérez-Prieto J, Sanaú M. Adv. Synth. Catal. 2008; 350: 234

    • For a recent example of a Z-selective head-to-head dimerization, see:
    • 4c Jahier C, Zatolochnaya OV, Zvyagintsev NV, Ananikov VP, Gevorgyan V. Org. Lett. 2012; 14: 2846

    • For a recent example of head-to-tail selective cross dimerization, see:
    • 4d Xu H.-D, Zhang R.-W, Li X, Huang S, Tang W, Hu W.-H. Org. Lett. 2013; 15: 840
    • 5a Trost BM, Chan C, Rühter G. J. Am. Chem. Soc. 1987; 109: 3486
    • 5b Trost BM, Sorum MT, Chan C, Harms AE, Rühter G. J. Am. Chem. Soc. 1997; 119: 698
  • 6 Dash AK, Eisen MS. Org. Lett. 2000; 2: 737
    • 7a Boese WT, Goldman AS. Organometallics 1991; 10: 782
    • 7b Lee C.-C, Lin Y.-C, Liu Y.-H, Wang Y. Organometallics 2005; 24: 136
    • 7c Peng HM, Zhao J, Li X. Adv. Synth. Catal. 2009; 351: 1371
    • 8a Gao Y, Puddephat RJ. Inorg. Chim. Acta 2003; 350: 101
    • 8b Melis K, De Vos D, Jacobs P, Verpoort F. J. Organomet. Chem. 2003; 671: 131
    • 8c Baratta W, Herrmann WA, Rigo P, Schwarz J. J. Organomet. Chem. 2000; 593-594: 489
    • 9a Heeres HJ, Teuben JH. Organometallics 1991; 10: 782
    • 9b Duchateau R, van Wee CT, Teuben JH. Organometallics 1996; 15: 2291
    • 9c Nishiura M, Hou Z. J. Mol. Catal. A: Chem. 2004; 213: 101
  • 10 Sun S, Kroll J, Luo Y, Zhang L. Synlett 2012; 23: 54
  • 11 Kondo M, Kochi T, Kakiuchi F. J. Am. Chem. Soc. 2011; 133: 32
  • 12 Sakai K, Kochi T, Kakiuchi F. Org. Lett. 2011; 13: 3928
  • 13 Sakai K, Kochi T, Kakiuchi F. Org. Lett. 2013; 15: 1024
  • 14 Yu X, Ren H, Xiao Y, Zhang J. Chem. Eur. J. 2008; 14: 8481

    • The difficulty in isolation of 3a has been commented:
    • 15a Ohshita J, Furumori K, Matsuguchi A, Ishikawa M. J. Org. Chem. 1990; 55: 3277
    • 15b Carlton L, Read G. J. Chem. Soc., Perkin Trans. 1 1978; 1631
  • 16 When the reaction was carried out using only one of the two phosphines, TDMPP or P(p-anis)3, the cyclization reaction did not take place.