Subscribe to RSS
DOI: 10.1055/s-2008-1042926
Butyltellurium Tribromide: A Suitable Electrophilic Source to Cyclization Reactions
Publication History
Publication Date:
11 March 2008 (online)
Abstract
We present here our results of the electrophilic cyclization reaction of (Z)-chalcogenoenynes using butyltellurium tribromide as an electrophilic source. The cyclization reaction proceeded cleanly under mild reaction conditions and 3-(butyltellanyl)chalcogenophenes were formed in moderate to excellent yields. Subsequent, using these heterocycles as substrate to palladium-catalyzed cross-coupling reactions a new carbon-carbon bond was formed in good yields.
Key words
tellurium - electrophilic cyclization - chalcogenophenes
- For representative illustrations, see the following reviews:
-
1a
Nakamura I.Yamamoto Y. Chem. Rev. 2004, 104: 2127 -
1b
Zeni G.Larock RC. Chem. Rev. 2004, 104: 2285 -
1c
Alonso F.Beletskaya IP.Yus M. Chem. Rev. 2004, 104: 3079 -
1d
Vizer SA.Yerzhanov KB.Al Aziz Al Quntar A.Dembitsky VM. Tetrahedron 2004, 60: 5499 -
2a
Barluenga J.Trincado M.Rubio E.Gonzalez JM. Angew. Chem. Int. Ed. 2003, 42: 2406 -
2b
Yue D.Yao T.Larock RC. J. Org. Chem. 2006, 71: 62 -
2c
Yue D.Yao T.Larock RC. J. Org. Chem. 2005, 70: 10292 -
2d
Arcadi A.Cacchi S.Fabrizi G.Marinelli F.Moro L. Synlett 1999, 1432 -
2e
Yue D.Larock RC. J. Org. Chem. 2002, 67: 1905 -
2f
Hessian KO.Flynn BL. Org. Lett. 2003, 5: 4377 -
2g
Kesharwani T.Worlikar SA.Larock RC. J. Org. Chem. 2006, 71: 2307 -
2h
Flynn BL.Flynn GP.Hamel E.Jung MK. Bioorg. Med. Chem. Lett. 2001, 11: 2341 -
2i
Sniady A.Wheeler KA.Dembinski R. Org. Lett. 2005, 7: 1769 -
2j
Knight DW.Redfern AL.Gilmore J. J. Chem. Soc., Perkin Trans. 1 2002, 622 -
2k
Huang Q.Hunter JA.Larock RC.
J. Org. Chem. 2002, 67: 3437 -
2l
Yue D.Della Ca N.Larock RC. Org. Lett. 2004, 6: 1581 -
2m
Yao T.Larock RC. J. Org. Chem. 2005, 70: 1432 -
2n
Yao T.Campo MA.Larock RC. J. Org. Chem. 2005, 70: 3511 -
2o
Zhou C.Dubrovsky AV.Larock RC. J. Org. Chem. 2006, 71: 1626 -
2p
Waldo JP.Larock RC. Org. Lett. 2005, 7: 5203 -
2q
Arcadi A.Cacchi S.Giuseppe SD.Fabrizi G.Marinelli F. Org. Lett. 2002, 4: 2409 -
2r
Peng A.Ding Y. J. Am. Chem. Soc. 2003, 125: 15006 -
2s
Zeni G.Ludtke DS.Panatieri RB.Braga AL. Chem. Rev. 2006, 106: 1032 -
2t
Zeni G.Braga AL.Stefani HA. Acc. Chem. Res. 2003, 36: 731 -
3a
Shiah HS.Lee WS.Juang SH.Hong PC.Lung CC.Chang CJ.Chou KM.Chang JY. Biochem. Pharmacol. 2007, 73: 610 -
3b
Juang SH.Lung CC.Hsu PC.Hsu KS.Li YC.Hong PC.Shiah HS.Kuo CC.Huang CW.Wang YC.Huang L.Chen TS.Chen SF.Fu KC.Hsu CL.Lin MJ.Chang CJ.Ashendel CL.Chan TCK.Chou KM.Chang JY. Mol. Cancer Ther. 2007, 6: 193 -
3c
Shiah HS.Lee WS.Juang SH.Chang CJ.Chang JY. Clin. Cancer Res. 2005, 11: 9101S - 4
Alves D.Luchese C.Nogueira CW.Zeni G. J. Org Chem. 2007, 72: 6726 -
5a
Zeni G.Ludtke DS.Panatieri RB.Braga AL. Chem. Rev. 2006, 106: 1032 -
5b
Zeni G.Braga AL.Stefani HA. Acc. Chem. Res. 2003, 36: 731 ; and references cited therein - 6
Petragnani N.Stefani HA. In Tellurium in Organic Synthesis 2nd ed.: Academic Press; London: 2007. - 7
Stefani HA.Petragnani N.Zukerman-Schpector J.Dornelles L.Silva DO.Braga AL. J. Organomet. Chem. 1998, 562: 127 -
9a
Miyaura N.Suzuki A. Chem. Rev. 1995, 95: 2457 -
9b
Molander GA.Ellis N. Acc. Chem. Res. 2007, 40: 275 -
9c
Stefani HA.Cella R.Vieira AS. Tetrahedron 2007, 63: 3623 -
9d
Stefani HA.Cella R.Dorr FA.Pereira CMP.Zeni G.Gomes M. Tetrahedron Lett. 2005, 46: 563 -
9e
Cella R.Cunha RLOR.Reis AES.Pimenta DC.Klitzke CF.Stefani HA. J. Org. Chem. 2006, 71: 244 - 10
Barancelli DA.Alves D.Prediger P.Stangherlin EC.Nogueira CW.Zeni G. Synlett 2008, 119
References and Notes
General Procedure for the BuTeBr
3
Cyclizations
To a solution of 0.50 mmol of the appropriate (Z)-selenoenyne in MeCN (5 mL) was added BuTeBr3 (0.233 g, 0.55 mmol). The reaction mixture was allowed to stir at r.t. for the time showed in Table
[3]
. After this time, EtOH (5 mL) and NaBH4 (0.037 g, 1 mmol) were added under vigorous stirring (gas evolution was observed during this addition). The reaction mixture was stirred at r.t. for one additional hour, diluted with EtOAc (20 mL) and washed with H2O (10 mL) and brine (3 × 10 mL). The organic layer was dried over anhyd Mg2SO4 and concentrated under vacuum to yield the crude product, which was purified by flash chromatography on silica gel using hexane as the eluent.
Analysis of the 1H NMR and 13C NMR spectra showed that all the obtained products presented data in full agreement with their assigned structures.
Selected Spectral and Analytical Data for 2b
Yield 0.212g (91%). 1H NMR (200 MHz, CDCl3): δ = 7.51-7.49 (m, 5 H), 7.44-7.28 (m, 6 H), 2.79 (t, J = 7.6 Hz, 2 H), 1.67 (quin, J = 7.6 Hz, 2 H), 1.29 (sext, J = 7.6 Hz, 2 H), 0.84 (t, J = 7.6 Hz, 3 H). 13C NMR (100 MHz, CDCl3): δ = 150.92, 150.21, 137.67, 135.75, 135.14, 129.31, 128.93, 128.25, 127.97, 127.76, 126.20, 104.55, 36.64, 24.88, 13.32, 8.88. MS: m/z (rel. intensity) = 468 (37), 411 (11), 284 (72), 202 (100), 77 (6), 57 (5). HRMS: m/z calcd for C20H20SeTe: 469.9792; found: 469.9798.