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-
For literature examples see (a) using a lithium amide: S. G. Davies, I. M. Dordor-Hedgecock, K. H. Sutton and J. C. Walker, Tetrahedron Lett., 1986, 27, 3787; (b) using a titanium amide: A. Hosomi, T. Yanagi and M. Hojo, Tetrahedron Lett., 1991, 32, 2371.
-
(1986)
Tetrahedron Lett.
, vol.27
, pp. 3787
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-
Davies, S.G.1
Dordor-Hedgecock, I.M.2
Sutton, K.H.3
Walker, J.C.4
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31
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0025896618
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-
For literature examples see (a) using a lithium amide: S. G. Davies, I. M. Dordor-Hedgecock, K. H. Sutton and J. C. Walker, Tetrahedron Lett., 1986, 27, 3787; (b) using a titanium amide: A. Hosomi, T. Yanagi and M. Hojo, Tetrahedron Lett., 1991, 32, 2371.
-
(1991)
Tetrahedron Lett.
, vol.32
, pp. 2371
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-
Hosomi, A.1
Yanagi, T.2
Hojo, M.3
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32
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-
2442710051
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Lithium N-benzyl-N-α-methylbenzylamide adds to α,β- unsaturated N-acyloxazolidinones in the anti-s-cis conformation: S. G. Davies, G. Hermann, A. D. Smith and M. J. Sweet, Chem. Commun., 2004, 1128.
-
(2004)
Chem. Commun.
, pp. 1128
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-
Davies, S.G.1
Hermann, G.2
Smith, A.D.3
Sweet, M.J.4
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33
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0000310559
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Kuzuya et al. have shown that 2-pyridone effects a rate enhancement upon mutarotation of glucose, thought to be due to its ability to act as both a base and an acid simultaneously: M. Kuzuya, A. Noguchi and T. Okuda, Bull. Chem. Soc. Jpn, 1984, 57, 3461.
-
(1984)
Bull. Chem. Soc. Jpn.
, vol.57
, pp. 3461
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-
Kuzuya, M.1
Noguchi, A.2
Okuda, T.3
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34
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11144276124
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Amide and carbamate proton sources have been used widely in the literature; for selected examples see: K. Tomioka and H. Fujihara, J. Chem. Soc., Perkin Trans. 1, 1999, 2377; D. R. Carbery and T. J. Donohoe, Chem. Commun., 2004, 722.
-
(1999)
J. Chem. Soc., Perkin Trans. 1
, pp. 2377
-
-
Tomioka, K.1
Fujihara, H.2
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35
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1842483974
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Amide and carbamate proton sources have been used widely in the literature; for selected examples see: K. Tomioka and H. Fujihara, J. Chem. Soc., Perkin Trans. 1, 1999, 2377; D. R. Carbery and T. J. Donohoe, Chem. Commun., 2004, 722.
-
(2004)
Chem. Commun.
, pp. 722
-
-
Carbery, D.R.1
Donohoe, T.J.2
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