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Synthesis 2004(17): 2821-2824
DOI: 10.1055/s-2004-834857
DOI: 10.1055/s-2004-834857
PAPER
© Georg Thieme Verlag Stuttgart · New YorkAn Efficient Stereoselective Synthesis of (E)-β-Fluoroalkenyliodonium Salts
Further Information
Received
24 June 2004
Publication Date:
07 October 2004 (online)
Publication History
Publication Date:
07 October 2004 (online)

Abstract
Stereoselective synthesis of (E)-β-fluoroalkenyliodonium salts was performed by the treatment of alk-1-ynes with p-iodotoluene difluoride in the presence of HBF4-Et2O. The reaction occurred instantaneously at -78 °C to give the fluoroalkenyliodonium salts in good yields with high stereoselectivity. The Pd-catalyzed carbomethoxylation of the fluoroalkenyliodonium salt was also carried out to obtain a (E)-β-fluoro-α,β-unsaturated ester.
Key words
iodonium salt - fluoroalkene - p-iodotoluene difluoride - stereoselective synthesis - fluorination reaction
- 1a
Welch JT.Eswarakrishnan S. Fluorine in Bioorganic Chemistry Wiley; New York: 1991. - 1b
Welch JT. Tetrahedron 1987, 43: 3123 - 1c
Ismail FMD. J. Fluorine Chem. 2002, 118: 27 - 1d
Smart BE. J. Fluorine Chem. 2001, 109: 3 - 2a
Kim BT.Min YK.Asami T.Park NK.Kwon OY.Cho KY.Yoshida S. Tetrahedron Lett. 1997, 38: 1797 - 2b
Masnyl M.Fried J. Tetrahedron Lett. 1989, 30: 3243 - 2c
Grieco PA.Takigawa T.Vedananda TR. J. Org. Chem. 1985, 50: 3111 - 2d
Grieco PA.Schillinger WJ.Yokoyama Y. J. Med. Chem. 1980, 23: 1077 - 3a
Okada M.Nakamura Y.Saito A.Sato A.Horikawa H.Taguchi T. Tetrahedron Lett. 2002, 43: 5845 - 3b
Otaka A.Watanabe H.Yukimasa A.Oishi S.Tamamura H.Fujii N. Tetrahedron Lett. 2001, 42: 5443 - 3c
Peng S.Qing F.-L.Li Y.-Q.Hu C.-M. J. Org. Chem. 2000, 65: 694 - 3d
Huang X.-H.He P.-Y.Shi G.-Q. J. Org. Chem. 2000, 65: 627 - 3e
Brown SJ.Corr S.Percy JM. Tetrahedron Lett. 2000, 41: 5269 - 3f
Chevrie D.Lequeux T.Pommelet J.-C. Org. Lett. 1999, 1: 1539 - 3g
Percy JM.Prime ME. J. Fluorine Chem. 1999, 100: 147 - 3h
Lin J.Welch JT. Tetrahedron Lett. 1998, 39: 9613 - 3i
Percy JM.Wilkes RD. Tetrahedron 1997, 53: 14749 - 3j
Hossain MA. Tetrahedron Lett. 1997, 38: 49 - 3k
Kuroboshi M.Yamada N.Takebe Y.Hiyama T. Tetrahedron Lett. 1995, 36: 6271 - 3l
Clemenceau D.Cousseau J. Tetrahedron Lett. 1993, 34: 6903 - 3m
Gillet JP.Sauvêtre R.Normant JF. Synthesis 1982, 297 - 4a
Zhang X.Burton DJ. J. Fluorine Chem. 2001, 112: 317 - 4b
Chen C.Wilcoxen K.Zhu Y.-F.Kim K.-I.McCarthy JR. J. Org. Chem. 1999, 64: 3476 - 4c
Burton DJ. J. Fluorine Chem. 1999, 100: 177 - 4d
Chen C.Wilcoxen K.Strack N.McCarthy JR. Tetrahedron Lett. 1999, 40: 827 - 4e
Percy E.Singh M.Takahashi T.Takeuchi Y.Kirk KL. J. Fluorine Chem. 1998, 91: 5 - 4f
McCarthy JR.Huber EW.Le T.-B.Laskovics FM.Matthews DP. Tetrahedron 1996, 52: 45 - 4g
Patrick TB.Lanahan MV.Yang C.Walker JK.Hutchinson CL.Neal BE. J. Org. Chem. 1994, 59: 1210 - 4h
Pirrung MC.Rowley EG.Holmes CP. J. Org. Chem. 1993, 58: 5683 - 4i
McCarthy JR.Matthews DP.Stemerick DM.Huber EW.Bey P.Lippert BJ.Snyder RD.Sunkara PS. J. Am. Chem. Soc. 1991, 113: 7539 - 4j
Burton DJ. J. Fluorine Chem. 1983, 23: 339 - 4k
Moghadam GE.Penne JS. Bull. Soc. Chim. Fr. 1985, 448 - 5a
Eddarir S.Francesch C.Mestdagh H.Rolando C. Bull. Soc. Chim. Fr. 1997, 134: 741 - 5b
Eddarir S.Mestdagh H.Rolando C. Tetrahedron Lett. 1991, 32: 69 - 6a
Carpenter W. J. Org. Chem. 1966, 31: 2688 - 6b Recent study:
Sawaguchi M.Ayuba S.Hara S. Synthesis 2002, 1802 - 7
Hara S.Yoshida M.Fukuhara T.Yoneda N. Chem. Commun. 1998, 965 - 8a
Hara S.Yamamoto K.Yoshida M.Fukuhara T.Yoneda N. Tetrahedron Lett. 1999, 40: 7815 - 8b
Yoshida M.Hara S.Fukuhara T.Yoneda N. Tetrahedron Lett. 2000, 41: 3887 - 8c
Yoshida M.Nagahara D.Fukuhara T.Yoneda N.Hara S. J. Chem. Soc., Perkin Trans. 1 2001, 2283 - 9 The stereochemistry was determined by 1H NMR. A vinylic hydrogen of 2a appeared at 6.70 ppm as a doublet (3
J
H-F = 14.4 Hz), which was in good agreement with the reported data of a (E)-β-fluoroalkenyliodonium salt; see ref.7 A larger coupling constant (3
J
H-F = 33.2 Hz) was observed from (Z)-2-fluorododecenyliodonium tetrafluoroborate:
Yoshida M.Hara S. Org. Lett. 2003, 5: 573 - 10a
Dehmlow EV.Lissel M. Liebigs Ann. Chem. 1980, 1: 1 - 10b
Brandsma L. Preparative Acetylenic Chemistry Elsevier; Amsterdam: 1971. - 10c
Khan NA. Org. Synth. Coll. Vol. IV Wiley; New York: 1963. p.969 - 10d
Brandsma L.Verkruijsse HD. Synthesis of Acetylenes, Allenes and Cumulenes Elsevier; Amsterdam: 1981.