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Artus, G.R.J.4
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14
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For non-racemic chiral imidazolium salts, see: (a) Tosoni, M.; Laschat, S.; Baro, A. Helv. Chim. Acta 2004, 87, 2742.
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(e) Earle, M. J.; McCormac, P. B.; Seddon, K. R. Green Chem. 1999, 1, 23.
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Earle, M.J.1
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Seddon, K.R.3
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19
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26844462863
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Ref. 5e
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To the best of our knowledge only two examples thereof exist: (a) Ref. 5e.
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20
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14744270265
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(b) Fukumoto, K.; Yoshizawa, M.; Ohno, H. J. Am. Chem. Soc. 2005, 127, 2398.
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Fukumoto, K.1
Yoshizawa, M.2
Ohno, H.3
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22
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26844453912
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note
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Presumably, methylimidazolium formation is due to Hoffmann type elimination. NMR spectroscopy of crude reaction mixtures indicated concomitant alkene formation.
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23
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0034700585
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For di- and polycationic ILs, see: Lall, S. I.; Mancheno, D.; Castro, S.; Behaj, V.; Cohen, J. I.; Engel, R. Chem. Commun. 2000, 2413.
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Lall, S.I.1
Mancheno, D.2
Castro, S.3
Behaj, V.4
Cohen, J.I.5
Engel, R.6
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24
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0000547940
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For chiral dicationic imidazolium salts, see: (a) Clyne, D. S.; Jin, J.; Genest, E.; Gallucci, J. C.; Rajan Babu, T. V. Org. Lett. 2000, 2, 1125.
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Clyne, D.S.1
Jin, J.2
Genest, E.3
Gallucci, J.C.4
Rajan Babu, T.V.5
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25
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3042670320
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(b) Marshall, C.; Ward, M. F.; Harrison, W. T. A. Tetrahedron Lett. 2004, 45, 5703.
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Marshall, C.1
Ward, M.F.2
Harrison, W.T.A.3
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26
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0030963592
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Howarth, J.; Hanlon, K.; Fayne, D.; McCormac, P. Tetrahedron Lett. 1997, 38, 3097.
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Howarth, J.1
Hanlon, K.2
Fayne, D.3
McCormac, P.4
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27
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26844471883
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note
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2O system is not possible.
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28
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26844559532
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note
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2O extraction method.
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30
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0000639359
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Wiley: New York
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Fieser, L. F.; Fieser, M. A. Reagents for Organic Synthesis, Vol. 1; Wiley: New York, 1967, 1179.
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Reagents for Organic Synthesis, Vol. 1
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Fieser, L.F.1
Fieser, M.A.2
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