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1
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34249987145
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Some recent synthetic applications of lateral lithiation include: and references cited therein.
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Some recent synthetic applications of lateral lithiation include:. Uchida K., Fukuda T., and Iwao M. Tetrahedron 63 (2007) 7178-7186 and references cited therein.
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(2007)
Tetrahedron
, vol.63
, pp. 7178-7186
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Uchida, K.1
Fukuda, T.2
Iwao, M.3
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3
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0035903837
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Burkhart D.J., Zhou P., Blumenfeld A., Twamley B., and Natale N.R. Tetrahedron 57 (2001) 8039-8046
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(2001)
Tetrahedron
, vol.57
, pp. 8039-8046
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Burkhart, D.J.1
Zhou, P.2
Blumenfeld, A.3
Twamley, B.4
Natale, N.R.5
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5
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0034608007
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Wang C.-C., Li J.J., Huang H.-C., Lee L.F., and Reitz D.B. J. Org. Chem. 65 (2000) 2711-2715
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(2000)
J. Org. Chem.
, vol.65
, pp. 2711-2715
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Wang, C.-C.1
Li, J.J.2
Huang, H.-C.3
Lee, L.F.4
Reitz, D.B.5
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10
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0034616006
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The MOM group supports lateral lithiation if ortho-lithiation is impossible, e.g.
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The MOM group supports lateral lithiation if ortho-lithiation is impossible, e.g.,. Yang D., Ye X.-Y., and Xu M. J. Org. Chem. 65 (2000) 2208-2217
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(2000)
J. Org. Chem.
, vol.65
, pp. 2208-2217
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Yang, D.1
Ye, X.-Y.2
Xu, M.3
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11
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0004316553
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The dianion derived directly from ortho-cresol has also been alkylated, see:
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The dianion derived directly from ortho-cresol has also been alkylated, see:. Andringa H., Verkruijsse H.D., Brandsma L., and Lochmann L. J. Organomet. Chem. 393 (1990) 307-314
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(1990)
J. Organomet. Chem.
, vol.393
, pp. 307-314
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Andringa, H.1
Verkruijsse, H.D.2
Brandsma, L.3
Lochmann, L.4
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13
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0032511947
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Clayden's group have used a carbamate to stabilise both lateral and ortho-lithiated species, see:
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Clayden's group have used a carbamate to stabilise both lateral and ortho-lithiated species, see:. Clayden J., Pink J.H., Westlund N., and Wilson F.X. Tetrahedron Lett. 39 (1998) 8377-8380
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(1998)
Tetrahedron Lett.
, vol.39
, pp. 8377-8380
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Clayden, J.1
Pink, J.H.2
Westlund, N.3
Wilson, F.X.4
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15
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31444441304
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Wilkinson J.A., Rossington S.B., Ducki S., Leonard J., and Hussain N. Tetrahedron 62 (2006) 1833-1844
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(2006)
Tetrahedron
, vol.62
, pp. 1833-1844
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Wilkinson, J.A.1
Rossington, S.B.2
Ducki, S.3
Leonard, J.4
Hussain, N.5
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17
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0141670408
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For a review of structural aspects of lateral and ortho-lithiated benzene derivatives, see:
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For a review of structural aspects of lateral and ortho-lithiated benzene derivatives, see:. Wheatley A. Eur. J. Inorg. Chem. (2003) 3291-3303
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(2003)
Eur. J. Inorg. Chem.
, pp. 3291-3303
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Wheatley, A.1
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20
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35148855038
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Raiber E.-A., Wilkinson J.A., Manetti F., Botta M., Deakin J., Gallagher J., Lyon M., and Ducki S. Bioorg. Med. Chem. Lett. 17 (2007) 6321-6325
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(2007)
Bioorg. Med. Chem. Lett.
, vol.17
, pp. 6321-6325
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Raiber, E.-A.1
Wilkinson, J.A.2
Manetti, F.3
Botta, M.4
Deakin, J.5
Gallagher, J.6
Lyon, M.7
Ducki, S.8
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21
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5644297285
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Additions of organolithium species to epoxides:. Rapoport Z., and Marek I. (Eds), Wiley and Sons, New York, NY
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Additions of organolithium species to epoxides:. Chemla F., and Vrancken E. In: Rapoport Z., and Marek I. (Eds). The Chemistry of Organolithium Reagents (2004), Wiley and Sons, New York, NY 1165-1242
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(2004)
The Chemistry of Organolithium Reagents
, pp. 1165-1242
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Chemla, F.1
Vrancken, E.2
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22
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33645778110
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Reactions involving laterally lithiated benzenoid aromatics:
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Reactions involving laterally lithiated benzenoid aromatics:. Clayden J., Stimson C.C., Helliwell M., and Keenan M. Synlett (2006) 873-876
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(2006)
Synlett
, pp. 873-876
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Clayden, J.1
Stimson, C.C.2
Helliwell, M.3
Keenan, M.4
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24
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0030013628
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Reich S.H., Melnick M., Pino M.J., Fuhry M.-A.M., Trippe A.J., Appelt K., Davies J.F., Wu B.-W., and Musick L. J. Med. Chem. 39 (1996) 2781-2794
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(1996)
J. Med. Chem.
, vol.39
, pp. 2781-2794
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Reich, S.H.1
Melnick, M.2
Pino, M.J.3
Fuhry, M.-A.M.4
Trippe, A.J.5
Appelt, K.6
Davies, J.F.7
Wu, B.-W.8
Musick, L.9
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25
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12944334176
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For example:
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For example:. Ortiz R., and Yus M. Tetrahedron 61 (2005) 1699-1707
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(2005)
Tetrahedron
, vol.61
, pp. 1699-1707
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Ortiz, R.1
Yus, M.2
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