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1
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84952142578
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For recent reviews on the synthesis of heterocyclic compounds by aza-Wittig reaction, see a) S. Eguchi, Y. Matsushita, and K. Yamashita, Org. Prep. Proced. Int., 24, 209 (1992);
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Org. Prep. Proced. Int.
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Eguchi, S.1
Matsushita, Y.2
Yamashita, K.3
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4
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0000416574
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d) H. Wamhoff, G. Rechardt, and S. Stölben, Avances in Heterocyclic Chemistry, Vol. 64, p. 159 (1996).
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Avances in Heterocyclic Chemistry
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Wamhoff, H.1
Rechardt, G.2
Stölben, S.3
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5
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-
0000363937
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For recent reviews on iminophosphoranes, see a) Y. G. Gololobov, I. N. Zhmurova, and L. F. Kasukhin, Tetrahedron, 37, 437 (1981);
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(1981)
Tetrahedron
, vol.37
, pp. 437
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Gololobov, Y.G.1
Zhmurova, I.N.2
Kasukhin, L.F.3
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7
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-
0000882290
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Five-membered compounds: a) H. Takeuchi, S. Yanagida, T. Ozaki, S. Hagiwara, and S. Eguchi, J. Org. Chem., 54, 431 (1989);
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Takeuchi, H.1
Yanagida, S.2
Ozaki, T.3
Hagiwara, S.4
Eguchi, S.5
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8
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0001134741
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b) H. Takeuchi, S. Hagiwara, and S. Eguchi, Tetrahedron, 45, 6375 (1989);
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Tetrahedron
, vol.45
, pp. 6375
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Takeuchi, H.1
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Eguchi, S.3
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9
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37049075392
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c) S. Eguchi and H. Takeuchi, J. Chem Soc., Chem. Commum., 1989, 602, Six-membered compounds:
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J. Chem Soc., Chem. Commum.
, vol.1989
, pp. 602
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Eguchi, S.1
Takeuchi, H.2
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11
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0001695638
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c) H. Takeuchi, Y. Matsushita, and S. Eguchi, J. Org. Chem., 56, 1535 (1991);
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Takeuchi, H.1
Matsushita, Y.2
Eguchi, S.3
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12
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16044368365
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f) S. Eguchi, H. Takeuchi, and Y. Matsushita, Heterocycles, 33, 153 (1992);
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Heterocycles
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Eguchi, S.1
Takeuchi, H.2
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13
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0043026193
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g) S. Eguchi, Y. Matsushita, and H. Takeuchi, J. Org. Chem., 57, 6576 (1992);
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J. Org. Chem.
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Eguchi, S.1
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Takeuchi, H.3
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15
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0001563990
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i) S. Eguchi, K. Yamashita, and Y. Matsushita, Synlett, 1992, 295;
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Synlett
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Eguchi, S.1
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Matsushita, Y.3
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16
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0029009886
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j) S. Eguchi, K. Yamashita, Y. Matsushita, and A. Kakchi, J. Org. Chem., 60, 4006 (1995);
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Eguchi, S.1
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Kakchi, A.4
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17
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0028904862
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k) P. Molina, I. Díaz, and A. Tárraga, Tetrahedron, 51, 5617 (1995);
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Molina, P.1
Díaz, I.2
Tárraga, A.3
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18
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0026555121
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l) J. Kurita, T. Iwata, S. Yasuike, and T. Tsuchiya, J. Chem. Soc., Chem. Commun., 1992, 81;
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J. Chem. Soc., Chem. Commun.
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Kurita, J.1
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Tsuchiya, T.4
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24
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0000592260
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b) D. R. Metha, J. S. Naravane, and R. M. Desai, J. Org. Chem., 28, 445 (1963).
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Metha, D.R.1
Naravane, J.S.2
Desai, R.M.3
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25
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0043026189
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note
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+, 45), 213 (1), 185 (100).
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-
-
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26
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0041523391
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The isolated 3a was hydrolyzed to 4a in HCl/THF at room temperature for 3 h (quantitative yield)
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The isolated 3a was hydrolyzed to 4a in HCl/THF at room temperature for 3 h (quantitative yield).
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