RSS-Feed abonnieren
Bitte kopieren Sie die angezeigte URL und fügen sie dann in Ihren RSS-Reader ein.
https://www.thieme-connect.de/rss/thieme/de/10.1055-s-00000084.xml
Synthesis 2013; 45(15): 2088-2092
DOI: 10.1055/s-0033-1338471
DOI: 10.1055/s-0033-1338471
special topic
Rhodium-Catalyzed Dimerization of Arylacetylenes and Addition of Malonates to 1,3-Enynes
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.
Key words
rhodium catalyst - aromatic terminal alkynes - head-to-tail dimerization - cyclopentene derivatives - allene derivativesSupporting Information
- for this article is available online at http://www.thieme-connect.com/ejournals/toc/synthesis.
- Supporting Information
-
References
- 1 Modern Acetylene Chemistry . Stang PJ, Diederich F. VCH; Weinheim: 1995
-
2 Trost BM. Science 1991; 254: 1471
- 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
- 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
- 4c Jahier C, Zatolochnaya OV, Zvyagintsev NV, Ananikov VP, Gevorgyan V. Org. Lett. 2012; 14: 2846
- 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
- 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.
For reviews, see:
For examples of E-selective head-to-head dimerization, see:
For a recent example of a Z-selective head-to-head dimerization, see:
For a recent example of head-to-tail selective cross dimerization, see:
The difficulty in isolation of 3a has been commented: