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Synthesis 2008(7): 1045-1048
DOI: 10.1055/s-2008-1032122
DOI: 10.1055/s-2008-1032122
PAPER
© Georg Thieme Verlag Stuttgart · New YorkSynthesis and Structure of Carbomethoxyethynyl[2.2]paracyclophane Derivatives
Further Information
Received
12 November 2007
Publication Date:
06 March 2008 (online)
Publication History
Publication Date:
06 March 2008 (online)

Abstract
The synthesis of the three ethynyl esters and three ethynyl[2.2]paracyclophane derivatives is described. All of the compounds were fully characterized.
Key words
cyclophanes - synthesis - Diels-Alder reaction - cross-coupling - alkynes
- 1a
Vögtle F. Cyclophane Chemistry Wiley & Sons; Chichester (UK): 1993. - 1b
Modern Cyclophane Chemistry
Gleiter R.Hopf H. Wiley-VCH; Weinheim: 2004. - 1c
Hopf H. Classics in Hydrocarbon Chemistry Wiley-VCH; Weinheim: 2000. - 1d
Gibson SE.Knight JD. Org. Biomol. Chem. 2003, 1: 1256 - 1e
Hong JW.Woo HY.Liu B.Bazan GC. J. Am. Chem. Soc. 2005, 127: 7435 ; and references cited therein - 1f
Popova EL.Rozenberg VI.Starikova ZA.Keuker-Baumann S.Kitzerow H.-Z.Hopf H. Angew. Chem. Int. Ed. 2002, 41: 3411 - 1g
Morisaki Y.Chujo Y. Macromolecules 2004, 37: 4099 - 1h
Guyard L.Nguyen DAM.Audebert P. Adv. Mater. 2001, 13: 133 - 1i
Salhi F.Collard DM. Adv. Mater. 2003, 15: 81 - 1j
Rozenberg VI.Danilova TI.Sergeeva Y.Shouklov IA.Starikova ZA.Hopf H.Sankararaman S.Dix I.Jones PG.Alt HG.Licht A. Eur. J. Inorg. Chem. 2002, 123 - 2a
Marrocchi A.Minuti L.Taticchi A.Dix I.Hopf H.Jones PG.Gacs-Baitz E. Eur. J. Org. Chem. 2001, 22: 4259 - 2b
Minuti L.Taticchi A.Lanari D.Marrocchi A.Gacs-Baitz E. Tetrahedron: Asymmetry 2003, 14: 2387 - 2c
Minuti L.Taticchi A.Marrocchi A.Lanari D.Tesei I.Gacs-Baitz E. Tetrahedron 2004, 60: 11759 - 2d
Minuti L.TaticchiA .Marrocchi A.Landi S.Gacs-Baitz E. Tetrahedron Lett. 2005, 46: 5735 - 2e
Valentini L.Mengoni F.Taticchi A.Marrocchi A.Kenny JM. J. Mater. Chem. 2006, 16: 1622 - 2f
Valentini L.Mengoni F.Kenny JM.Marrocchi A.Taticchi A. Small 2007, 3: 1200 - 3
Fringuelli F.Taticchi A. Diels-Alder Reaction. Selected Practical Methods Wiley & Sons; New York: 2002. - 4a
Guiry PJ.Mc Carthy M.Lacey PM.Sanders CP.Kelly S.Connolly DJ. Curr. Org. Chem. 2000, 4: 821 - 4b
Pu L. Chem. Rev. 1998, 98: 2405 - 5
Bondarenko L.Dix I.Hinrichs H.Hopf H. Synthesis 2004, 2751 - 6
Dix I. Ph.D. Dissertation Technical University Braunschweig; Germany: 2002. - 7
Pearson AJ.Kim JB. Tetrahedron Lett. 2003, 44: 8525 - 8
Sonogashira K. Metal-Catalyzed Cross-Coupling Reactions Wiley-VCH; Weinheim: 1998. - 9
Nesterov EE.Zhu Z.Swager T. J. Am. Chem. Soc. 2005, 127: 10083 - 10a
Takahashi S.Kuroyama Y.Sonogashira K.Hagihara N. Synthesis 1980, 8: 627 - 10b
Kosynkin DV.Tour JM. Org. Lett. 2001, 3: 993 - 10c
Loupy A.Sansoulet J.Vaziri-Zand F. Bull. Soc. Chim. Fr. 1987, 6: 1027 - 10d
McKenna MD.Barberà J.Marcos M.Serrano JL. J. Am. Chem. Soc. 2005, 127: 619 - 11
Sun S.-S.Sariciftci NS. Organic Photovoltaics. Mechanisms, Materials and Devices Taylor & Francis; Boca Raton (FL): 2005. - 12
Müller S.Liepold B.Roth GJ.Bestmann H.-J. Synlett 1996, 521