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DOI: 10.1055/s-2006-942437
DABCO-Catalyzed Reaction of Phenols or 1,2-Diphenols with Activated Alkynes Leading to the Formation of Alkenoic Acid Esters or 1,3-Dioxole Derivatives
Publikationsverlauf
Publikationsdatum:
26. Juni 2006 (online)

Abstract
The reaction of phenols or 1,2-diphenols with activated alkynes took place smoothly and rapidly in the presence of a catalytic amount of 1,4-diazabicyclo[2.2.2]octane (DABCO) at room temperature and resulted in the formation of various alkenoic acid esters or 1,3-dioxole derivatives in excellent yields. The scope and limitations, together with a plausible mechanism of the reaction are disclosed in this paper.
Key words
phenoles - 1,2-diphenoles - activated alkynes - alkenoic acid esters - 1,3-dioxoles
- 1 
             
            Winterfeldt E. Angew. Chem., Int. Ed. Engl. 1967, 6: 424
- 2a 
             
            Tebby JC.Wilson IF.Griffiths DV. J. Chem. Soc., Perkin Trans. 1 1979, 2133
- 2b 
             
            Butterfield PJ.Tebby JC.Griffiths DV. J. Chem. Soc., Perkin Trans. 1 1979, 1189
- 2c 
             
            Nozaki K.Ikeda K.Takaya H. J. Org. Chem. 1996, 61: 4516
- 2d 
             
            Nair V.Nair JS.Vinod AU. J. Chem. Soc., Perkin Trans. 1 1998, 3129
- 2e 
             
            Yavari I.Souri S.Sirouspour M.Djahaniani H.Nasiri F. Synthesis 2005, 1761
- 3a 
             
            Nair V.Pillai AN.Menon RS.Suresh E. Org. Lett. 2005, 7: 1189
- 3b 
             
            Nair V.Pillai AN.Beneesh PB.Suresh E. Org. Lett. 2005, 7: 4625
- 4a 
             
            Nair V.Menon RS.Deepthi A.Devi Rema B.Biju AT. Tetrahedron Lett. 2005, 46: 1337
- 4b 
             
            Yadav JS.Subba Reddy BV.Shubashree S.Sadashiv K.Naidu JJ. Synthesis 2004, 2376
- 4c 
             
            Nair V.Menon RS.Beneesh PB.Sreekumar V.Bindu S. Org. Lett. 2004, 6: 767
- 4d 
             
            Nair V.Vinod AU.Rajesh C. J. Org. Chem. 2001, 66: 4427
- 4e 
             
            Nair V.Vinod AU. Chem. Commun. 2000, 1019
- 5a 
             
            Shi Y.-L.Shi M. Org. Lett. 2005, 7: 3057
- 5b 
             
            Zhao G.-L.Shi Y.-L.Shi M. Org. Lett. 2005, 7: 4527
- 5c 
             
            Zhao G.-L.Shi M. J. Org. Chem. 2005, 70: 9975
- 5d 
             
            Ding H.Ma C.Yang Y.Wang Y. Org. Lett. 2005, 7: 2125
- 6a 
             
            Yang Z.Fan M.Mu R.Liang Y. Tetrahedron 2005, 61: 9140
- 6b 
             
            Fan M.Guo L.Liu X.Liu W.Liang Y. Synthesis 2005, 391
- 6c 
             
            Fan M.Yan Z.Liang Y. J. Org. Chem. 2005, 70: 8204
- 7a 
             
            Gudi MN.Hiriyakkanavar JG.George MV. Indian J. Chem. 1969, 7: 971
- 7b 
             
            Gupta RK.George MV. Tetrahedron 1975, 31: 1263
- 8a 
             
            Stoermer MJ.Fairlie DP. Aust. J. Chem. 1995, 48: 677
- 8b 
             
            Kodomari M.Sakamoto T.Yoshitomi S. J. Chem. Soc., Chem. Commun. 1990, 9: 701
- 9a 
             
            Nagarajan K.Rangarao V.Shah RK. Indian J. Chem. 1971, 9: 971
- 9b 
             
            Davies SG.Mobbs BE. J. Chem. Soc., Perkin Trans. 1 1987, 2597
- 11 
             
            Nozaki K.Sato N.Ikeda K.Takaya H. J. Org. Chem. 1996, 61: 4516
- 13 
             
            Winterfeldt E.Preuss H. Chem. Ber. 1966, 99: 450
References
Crystal data of 3 have been deposited in CCDC as deposition number 295601: C14H14O6, MW = 278.25, T = 296 (2) K, λ = 0.71073 Å, Monoclinic space group P2(1)/c, a = 10.046 (2) Å, b = 18.482 (4) Å, c = 7.566 (1) Å, α = 90.00°, β = 95.32 (2)°, γ = 90.00°, V = 1398.7 (5) Å3, Z = 4, D c = 1.321 mg/m3, µ = 0.104 mm-1, F(000) = 584, Crystal size 0.58 × 0.52 × 0.50 mm, Independent reflections 2600 [R(int) = 0.0103], Reflections collected 3009, Refinement method, full-matrix least-squares on F 2, Goodness-of-fit on F 2 1.083, Final R indices [I > 2σ(I)] R1 = 0.0387, wR2 = 0.1116, R indices (all data) R1 = 0.0627, wR2 = 0.1197, Extinction coefficient 0.119 (6), Largest diff. peak and hole 0.233 and -0.166 eÅ-3.
12Crystal data of 15 have been deposited in CCDC as deposition number 295602: C12H12O6, MW = 252.22, T = 296 (2) K, λ = 0.71073 Å, Orthorhombic space group Pbca, a = 7.314 (1) Å, b = 17.931 (4) Å, c = 18.351 (5) Å, α = 90.00°, β = 90.00°, γ = 90.00°, V = 2406.52 (67) Å3, Z = 8, D c = 1.392 mg/m3, µ = 0.113 mm-1, F(000) = 1056, Crystal size 0.60 × 0.34 × 0.34 mm, Independent reflections 2769 [R(int) = 0.0385], Reflections collected 3481, Refinement method, full-matrix least-squares on F 2, Goodness-of-fit on F 2 0.902, Final R indices [I > 2σ(I)] R1 = 0.0827, wR2 = 0.0975, R indices (all data) R1 = 0.0393, wR2 = 0.0879, Extinction coefficient 0.0098 (7), Largest diff. peak and hole 0.169 and -0.161 eÅ-3.
 
    