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Synthesis 2014; 46(04): 531-536
DOI: 10.1055/s-0033-1340346
DOI: 10.1055/s-0033-1340346
paper
Synthesis of m-Terphenyl Derivatives via Domino Diels–Alder/Retro-Diels–Alder Reaction of 1,3-Dienic δ-Sultones with Alkynes
Further Information
Publication History
Received: 27 August 2013
Accepted after revision: 12 November 2013
Publication Date:
02 January 2014 (online)
Dedicated to Dr. Margit Gruner on the occasion of her 65th birthday
Abstract
A highly regioselective synthetic method based on the domino Diels–Alder/retro-Diels–Alder reaction (DA/RDA) of 1,3-dienic δ-sultones with alkynes provides substituted m-terphenyls by elimination of SO3. A variety of δ-sultones and alkynes were examined to determine the scope of the reaction. The de novo synthesized aromatic products were obtained using thermal, microwave, and high-pressure activation.
Supporting Information
- for this article is available online at http://www.thieme-connect.com/ejournals/toc/synthesis.
- Supporting Information
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References
- 1 Kays DL. Dalton Trans. 2011; 40: 769
- 2 Goel A, Ram VJ. Tetrahedron 2009; 65: 7865
- 3 Kranjc K, Kocevar M. New J. Chem. 2005; 29: 1027
- 4 Kranjc K, Kocevar M. Curr. Org. Chem. 2010; 14: 1050
- 5 Alfini R, Cecchi M, Giomi D. Molecules 2010; 15: 1722
- 6 van der Plas HC. ARKIVOC 2008; (iii): 127
- 7 Aly AA. Org. Biomol. Chem. 2003; 1: 756
- 8 Gaitzsch J, Rogachev VO, Metz P, Yusubov MS, Filimonov VD, Kataeva O. J. Sulfur Chem. 2009; 30: 4
- 9 Rogachev VO, Yusubov MS, Filimonov VD. Russ. J. Org. Chem. 1999; 35: 415
- 10 Gaitzsch J, Rogachev V, Metz P, Filimonov VD, Zahel M, Kataeva O. J. Sulfur Chem. 2011; 32: 3
-
11 Chinchilla R, Najera C. Chem. Rev. 2007; 107: 874
- 12 Ziegler T, Layh M, Effenberger F. Chem. Ber. 1987; 120: 1347
- 13 Tanyeli C, Tarhan O. Synth. Commun. 1989; 19: 2453
- 14 Kappe CO. Angew. Chem. Int. Ed. 2004; 43: 6250
- 15 Kappe CO, Dallinger D. Mol. Diversity 2009; 13: 71
- 16 Benito-Lopez F, Egberink RJ, Reinhoudt DN, Verboom W. Tetrahedron 2008; 64: 10023
- 17 Kranjc K, Stefane B, Polanc S, Kocevar M. J. Org. Chem. 2004; 69: 3190
- 18 Yoshikai N, Mashima H, Nakamura E. J. Am. Chem. Soc. 2005; 127: 17978
- 19 Crystallographic data for the structure 11e have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication number CCDC 869138. These data can be obtained free of charge from the Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif or by writing to the Cambridge Crystallographic Data Centre, 12, Union Road, Cambridge CB2 1EZ, UK; fax: +44(1223)336033; E-mail: deposit@ccdc.cam.ac.uk.