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4
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0034699203
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For pertinent review for phenol synthesis, see: and references therein
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For pertinent review for phenol synthesis, see:. George T., Mabon R., Sweeney G., Sweeney J.B., and Tavassoli A. J. Chem. Soc., Perkin Trans. 1 (2000) 2529 and references therein
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J. Chem. Soc., Perkin Trans. 1
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George, T.1
Mabon, R.2
Sweeney, G.3
Sweeney, J.B.4
Tavassoli, A.5
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6
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0029936647
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Fujimoto K., Tokuda Y., Maekawa H., Matsubara Y., Mizuno T., and Nishiguchi I. Tetrahedron 52 (1996) 3889
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Tetrahedron
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Fujimoto, K.1
Tokuda, Y.2
Maekawa, H.3
Matsubara, Y.4
Mizuno, T.5
Nishiguchi, I.6
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8
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33746283734
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Burgo C.H., Barder T.E., Huang X., and Buchwald S.L. Angew. Chem., Int. Ed. 45 (2006) 4321
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(2006)
Angew. Chem., Int. Ed.
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Burgo, C.H.1
Barder, T.E.2
Huang, X.3
Buchwald, S.L.4
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13
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20544450502
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de Meijere A., and Diederich F. (Eds), Wiley-VCH, Weinheim
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In: de Meijere A., and Diederich F. (Eds). Metal-Catalyzed Cross-Coupling Reactions. 2nd ed. (2004), Wiley-VCH, Weinheim
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(2004)
Metal-Catalyzed Cross-Coupling Reactions. 2nd ed.
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14
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0033531744
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For an alternative two-step synthesis of phenols, see:
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For an alternative two-step synthesis of phenols, see:. Mann G., Incarvito C., Rheingold A.L., and Hartwig J.F. J. Am. Chem. Soc. 121 (1999) 3224
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(1999)
J. Am. Chem. Soc.
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Mann, G.1
Incarvito, C.2
Rheingold, A.L.3
Hartwig, J.F.4
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15
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33747793704
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During the preparation of the manuscript, a closely related and promising paper appeared.
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During the preparation of the manuscript, a closely related and promising paper appeared. Anderson K.W., Ikawa T., Tundel R.E., and Buchwald S.L. J. Am. Chem. Soc. 128 (2006) 10694-10695
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(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 10694-10695
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Anderson, K.W.1
Ikawa, T.2
Tundel, R.E.3
Buchwald, S.L.4
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16
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5044236958
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Kwong F.Y., Lam W.H., Yeung C.H., Chan K.S., and Chan A.S.C. Chem. Commun. (2004) 1922
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(2004)
Chem. Commun.
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Kwong, F.Y.1
Lam, W.H.2
Yeung, C.H.3
Chan, K.S.4
Chan, A.S.C.5
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18
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23844477550
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Kwong F.Y., Lai C.W., Yu M., Tan D.-M., Chan A.S.C., and Chan K.S. Organometallics 24 (2005) 4170
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(2005)
Organometallics
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Kwong, F.Y.1
Lai, C.W.2
Yu, M.3
Tan, D.-M.4
Chan, A.S.C.5
Chan, K.S.6
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20
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13244291383
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Macías F.A., Marín D., Oliveros-Bastidas A., Castellano D., Simonet A.M., and Molinillo J.M.G. J. Agric. Food Chem. 53 (2005) 538
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Macías, F.A.1
Marín, D.2
Oliveros-Bastidas, A.3
Castellano, D.4
Simonet, A.M.5
Molinillo, J.M.G.6
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22
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0035815141
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For the synthesis of tert-butyl aryl ether from ArX with NaOt-Bu, see:
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For the synthesis of tert-butyl aryl ether from ArX with NaOt-Bu, see:. Parrish C.A., and Buchwald S.L. J. Org. Chem. 66 (2001) 2498
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(2001)
J. Org. Chem.
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Parrish, C.A.1
Buchwald, S.L.2
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23
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33845476298
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note
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In fact, the electrophilic aryl halide is in situ transformed to nucleophile in the presence of base/water, and react with other electrophiles (for the two electrophilic components coupling reaction).
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