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1
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84956794765
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For a very recent review, see: A. Ricci. Weinheim: Wiley-VCH
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For a very recent review, see: Ricci A. Modern Amination Methods. 2000;Wiley-VCH, Weinheim.
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(2000)
Modern Amination Methods
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9
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0026697882
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Banks M.R., Blake A.J., Cadogan J.I.G., Dawson I.M., Gosney I., Grant K.J., Gaur S., Hodgson P.K.G., Knight K.S., Smith G.W., Stevenson D.E. Tetrahedron. 48:1992;7979-8006.
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(1992)
Tetrahedron
, vol.48
, pp. 7979-8006
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Banks, M.R.1
Blake, A.J.2
Cadogan, J.I.G.3
Dawson, I.M.4
Gosney, I.5
Grant, K.J.6
Gaur, S.7
Hodgson, P.K.G.8
Knight, K.S.9
Smith, G.W.10
Stevenson, D.E.11
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13
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0030718554
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Asymmetric cyclopropanation by an Oppolzer's sultam carbenoid was reported:
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Asymmetric cyclopropanation by an Oppolzer's sultam carbenoid was reported: Haddad N., Galili N. Tetrahedron: Asymmetry. 8:1997;3367-3370.
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(1997)
Tetrahedron: Asymmetry
, vol.8
, pp. 3367-3370
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Haddad, N.1
Galili, N.2
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14
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0343049646
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CAUTION: Reactions involving azides are capable of being explosive. While we have experienced no problems, care should be exercised
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CAUTION: Reactions involving azides are capable of being explosive. While we have experienced no problems, care should be exercised.
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15
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0342615502
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Lwowski W., de Mauriac R.A., Thompson M., Wilde R.E., Chen S.Y. J. Org. Chem. 40:1975;2608-2612.
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(1975)
J. Org. Chem.
, vol.40
, pp. 2608-2612
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Lwowski, W.1
De Mauriac, R.A.2
Thompson, M.3
Wilde, R.E.4
Chen, S.Y.5
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17
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0013473360
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For the reactivity of norbornene in the presence of different azides, see:
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For the reactivity of norbornene in the presence of different azides, see: Subbaraj A., Subba Rao O., Lwowski W. J. Org. Chem. 54:1989;3945-3952.
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(1989)
J. Org. Chem.
, vol.54
, pp. 3945-3952
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Subbaraj, A.1
Subba Rao, O.2
Lwowski, W.3
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18
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0030873707
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We isolated similar products by the cycloaddition reactions of different azides on sterically hindered enamines:
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We isolated similar products by the cycloaddition reactions of different azides on sterically hindered enamines: Fioravanti S., Pellacani L., Ricci D., Tardella P.A. Tetrahedron: Asymmetry. 8:1997;2261-2266.
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(1997)
Tetrahedron: Asymmetry
, vol.8
, pp. 2261-2266
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Fioravanti, S.1
Pellacani, L.2
Ricci, D.3
Tardella, P.A.4
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22
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0025601635
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The configuration of the major diastereomer was established by comparison with the same product obtained by elaboration of the appropriate optically pure trans-1,2-amino alcohol, according to a reported procedure:
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The configuration of the major diastereomer was established by comparison with the same product obtained by elaboration of the appropriate optically pure trans-1,2-amino alcohol, according to a reported procedure: Fioravanti S., Loreto M.A., Pellacani L., Tardella P.A. Tetrahedron: Asymmetry. 1:1990;931-936.
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(1990)
Tetrahedron: Asymmetry
, vol.1
, pp. 931-936
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Fioravanti, S.1
Loreto, M.A.2
Pellacani, L.3
Tardella, P.A.4
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24
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33746439764
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Svenstrup N., Bøgevig A., Hazell R.G., Jørgensen K.A. J. Chem. Soc., Perkin Trans. 1. 1999;1559-1566.
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(1999)
J. Chem. Soc., Perkin Trans. 1
, pp. 1559-1566
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Svenstrup, N.1
Bøgevig, A.2
Hazell, R.G.3
Jørgensen, K.A.4
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