RSS-Feed abonnieren
DOI: 10.1055/s-2002-31922
Synthesis of Cross-Conjugated Geminal Enediynes via Palladium Catalyzed Cross-Coupling Reaction of Ketene Butyltelluroacetals
Publikationsverlauf
Publikationsdatum:
07. Februar 2007 (online)
Abstract
The palladium-catalyzed cross coupling reaction of ketene butyltelluroacetals with terminal alkynes at room temperature affords cross-conjugated geminal enediynes in high yield under mild conditions.
Key words
cross-coupling - enynes - palladium - tellurium - ketene butyltellurocetals
-
1a
Heck RF. Org. React. 1982, 27: 345 -
1b
Negishi E.-I. Acc. Chem.Res. 1982, 27: 345 -
1c
Suzuki A. Pure Appl. Chem. 1985, 57: 1749 -
1d
Stille JK. Angew. Chem., Int. Ed. Engl. 1986, 25: 508 ; Angew. Chem. 1986, 98, 504 - 2
Sonogashira K. In Comprehensive Organic SynthesisTrost BM.Fleming I. Pergamon Press; New York: 1991. p.521 - 3
Nicolaou KC.Smith AL. In Modern Acetylene ChemistryStang PJ.Diederich F. VCH; Weinheim: 1995. p.253 - 4 Hird M., Gray G. W., Toyne K. J.; Mol. Cryst. Liq. Cryst.; 1991, 206: 187
-
5a
Comasseto JV.Ling LW.Petragnani N.Stefani HA. Synthesis 1997, 373 -
5b
Petragnani N. Tellurium in Organic Synthesis Academic Press; London: 1994. -
5c
Comasseto JV.Barrientos-Astigarraga RE. Aldrichimica Acta 2000, 33: 66 -
6a
Barros SM.Dabdoub MJ.Dabdoub VB.Comasseto JV. Organometallics 1989, 8: 1661 -
6b
Tucci FC.Chieffi A.Comasseto JV.Marino JP. J. Org. Chem. 1996, 61: 4975 -
6c
Dabdoub MJ.Dabdoub VB.Comasseto JV.Petragnani N. J. Organomet. Chem. 1986, 308: 211 -
6d
Dabdoub MJ.Dabdoub VB.Comasseto JV. Tetrahedron Lett. 1992, 33: 2261 -
6e
Zeni G.Formiga HB.Comasseto JV. Tetrahedron Lett. 2000, 41: 1311 -
6f
Zeni G.Chieffi A.Cunha RLOR.Zukerman-Schpector J.Stefani HA.Comasseto JV. Organometallics 1999, 18: 803 -
7a
Silveira CC.Perin G.Braga AL. Tetrahedron Lett. 1995, 36: 7361 -
7b
Silveira CC.Perin G.Braga AL.Dabdoub MJ.Jacob RG. Tetrahedron 1999, 55: 7421 - 8
Dabdoub MJ.Cassol TM.Barbosa SL. Tetrahedron Lett. 1996, 37: 831 - 9
Dabdoub MJ.Begnini ML.Guerrero PG. Tetrahedron 1998, 54: 2371 - 10
Braga AL.Zeni G.de Andrade LH.Silveira CC. Synlett 1997, 595 -
11a
Zeni G.Comasseto JV. Tetrahedron Lett. 1999, 40: 4619 -
11b
Zeni G.Menezes PH.Moro AV.Braga AL.Silveira CC.Stefani HA. Synlett 2001, 1473 -
11c
Zeni G.Panatieri RB.Lissner E.Menezes PH.Braga AL.Stefani HA. Org. Lett. 2001, 3: 819 -
11d
Zeni G.Nogueira CW.Panatieri RB.Silva DO.Menezes PH.Braga AL.Silveira CC.Stefani HA.Rocha JBT. Tetrahedron Lett. 2001, 42: 7921 -
11e
Braga AL.Zeni G.de Andrade LH.Silveira CC.Stefani HA. Synthesis 1998, 39 -
11f
Braga AL.Emmerich DJ.Silveira CC.Martins TL.Rodrigues OED. Synlett 2001, 369
References and Notes
Typical procedure for 8a: To a two-necked 25 mL round-bottomed flask under argon atmosphere containing PdCl2 (0.035 g, 20 mol%) and dry methanol (5 mL) was added the ketene butyltelluroacetal 6a (0.470g, 1 mmol). After stirring the mixture for 15 minutes at room temperature, 1-heptyne (0.192 g, 2 mmol) and Et3N (0.8 mL) were added. The reaction was stirred at room temperature for 4 h. After this time, the solids were filtered under vacuum, to the filtrate was added brine. The organics were extracted with dichloromethane (3 × 25 mL), dried over MgSO4 and concentrated under vacuum. The residue was purified by flash silica gel chromatography eluting with hexane; Yield 0.227 g (75%). Selected spectral and analytical data for 8a: 1H NMR (CDCl3, 200 MHz) δ(ppm): 7.86-7.82(m, 2 H), 7.33-7.30(m, 3 H), 6.89(s, 1 H), 2.42(t, 7.0 Hz, 2 H), 2.37(t, 7.0 Hz, 2 H), 1.75-1.20(m, 12 H), 0.96(t, 7.0 Hz, 3 H), 0.93(t, 7.0 Hz, 3 H); 13C NMR (CDCl3, 50 MHz) δ(ppm): 140.93, 135.99, 128.52, 128.38, 128.10, 104.08, 96.99, 88.92, 80.98, 78.61, 31.28, 31.14, 28.34, 28.01, 22.47, 22.22, 19.96, 19.80, 13.95, 13.80; IR (neat, cm-1): 3060, 2200, 2190, 1660, 786; LRMS (rel. int.) m/z 292(100), 178(80), 152(40), 91(50), 77(60).