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1
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56949090350
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Reviews:
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Reviews:
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8
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14544281506
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Qadir M., Cobb J., White A.J.P., Sheldrake P.W., Whittall N., Hii K.K., Horton P.N., and Hursthouse M.B. J. Org. Chem. 70 (2005) 1545-1551
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(2005)
J. Org. Chem.
, vol.70
, pp. 1545-1551
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Qadir, M.1
Cobb, J.2
White, A.J.P.3
Sheldrake, P.W.4
Whittall, N.5
Hii, K.K.6
Horton, P.N.7
Hursthouse, M.B.8
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9
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14544304543
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Qadir M., Cobb J., White A.J.P., Sheldrake P.W., Whittall N., Hii K.K., Horton P.N., and Hursthouse M.B. J. Org. Chem. 70 (2005) 1552-1557
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(2005)
J. Org. Chem.
, vol.70
, pp. 1552-1557
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Qadir, M.1
Cobb, J.2
White, A.J.P.3
Sheldrake, P.W.4
Whittall, N.5
Hii, K.K.6
Horton, P.N.7
Hursthouse, M.B.8
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10
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0037471462
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Qadir M., Priestley R.E., Rising T.D.W.F., Gelbrich T., Coles S.J., Hursthouse M.B., Sheldrake P.W., Whittall N., and Hii K.K. Tetrahedron Lett. 44 (2003) 3675-3678
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(2003)
Tetrahedron Lett.
, vol.44
, pp. 3675-3678
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Qadir, M.1
Priestley, R.E.2
Rising, T.D.W.F.3
Gelbrich, T.4
Coles, S.J.5
Hursthouse, M.B.6
Sheldrake, P.W.7
Whittall, N.8
Hii, K.K.9
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11
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33748670512
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Gibson S.E., Guillo N., Middleton R.J., Thuilliez A., and Tozer M.J. J. Chem. Soc., Perkin Trans. 1 (1997) 447-455
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(1997)
J. Chem. Soc., Perkin Trans. 1
, pp. 447-455
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Gibson, S.E.1
Guillo, N.2
Middleton, R.J.3
Thuilliez, A.4
Tozer, M.J.5
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13
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30544432647
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Kitamura Y., Hashimoto A., Yoshikawa S., Odaira J., Furuta T., Kan T., and Tanaka K. Synlett (2006) 115-117
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(2006)
Synlett
, pp. 115-117
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Kitamura, Y.1
Hashimoto, A.2
Yoshikawa, S.3
Odaira, J.4
Furuta, T.5
Kan, T.6
Tanaka, K.7
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14
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56949100198
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Optically pure MOP costs £58.80/50 mg (Sigma-Aldrich Catalogue 2008). rac-MOP is not commercially available.
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Optically pure MOP costs £58.80/50 mg (Sigma-Aldrich Catalogue 2008). rac-MOP is not commercially available.
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15
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56949108462
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For example, see:
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For example, see:
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19
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15044344246
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Microwave irradiation was employed for the synthesis of oxindoles by Pd-catalysed amidation reactions:
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Microwave irradiation was employed for the synthesis of oxindoles by Pd-catalysed amidation reactions:. Poondra R.R., and Turner N.J. Org. Lett. 87 (2005) 863-866
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(2005)
Org. Lett.
, vol.87
, pp. 863-866
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Poondra, R.R.1
Turner, N.J.2
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21
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56949101845
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For example, see:
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For example, see:
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22
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0001148752
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Chimirri A., Gitto R., Grasso S., Monforte A.M., Romeo G., and Zappala M. Heterocycles 36 (1993) 601-637
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(1993)
Heterocycles
, vol.36
, pp. 601-637
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Chimirri, A.1
Gitto, R.2
Grasso, S.3
Monforte, A.M.4
Romeo, G.5
Zappala, M.6
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23
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27144485239
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Yang T., Lin C.X., Fu H., Jiang Y.Y., and Zhao Y.F. Org. Lett. 7 (2005) 4781-4784
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(2005)
Org. Lett.
, vol.7
, pp. 4781-4784
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Yang, T.1
Lin, C.X.2
Fu, H.3
Jiang, Y.Y.4
Zhao, Y.F.5
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26
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33645782457
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One example of an intramolecular aryl amination can be found, where a highly substituted 8-membered heterocycle was prepared by Pd catalysis:
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One example of an intramolecular aryl amination can be found, where a highly substituted 8-membered heterocycle was prepared by Pd catalysis:. Neogi A., Majhi T.P., Mukhopadhyay R., Chattopadhyay, and P. J. Org. Chem. 71 (2006) 3291-3294
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(2006)
J. Org. Chem.
, vol.71
, pp. 3291-3294
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Neogi, A.1
Majhi, T.P.2
Mukhopadhyay, R.3
Chattopadhyay, P,4
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28
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0023202003
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Uchida I., Takase S., Kayakiri H., Kiyoto S., Hashimoto M., Tada T., Koda S., and Morimoto Y. J. Am. Chem. Soc. 109 (1987) 4108-4109
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(1987)
J. Am. Chem. Soc.
, vol.109
, pp. 4108-4109
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Uchida, I.1
Takase, S.2
Kayakiri, H.3
Kiyoto, S.4
Hashimoto, M.5
Tada, T.6
Koda, S.7
Morimoto, Y.8
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