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1
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0001586671
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Friedel-Crafts Alkylation
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Trost B.M., and Fleming I. (Eds), Pergamon, Oxford
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Olah G.A., Krishnamurit R., and Prakash G.K.S. Friedel-Crafts Alkylation. In: Trost B.M., and Fleming I. (Eds). Comprehensive Organic Synthesis Vol. 3 (1991), Pergamon, Oxford 293-339
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Olah, G.A.1
Krishnamurit, R.2
Prakash, G.K.S.3
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0036399737
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Barrett A.G.M., Bouloc N., Braddock D.C., Chadwick D., and Henderson D.A. Synlett 10 (2002) 1653
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Barrett, A.G.M.1
Bouloc, N.2
Braddock, D.C.3
Chadwick, D.4
Henderson, D.A.5
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9
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0035966593
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The loading of catalyst (Lewis acid) is usually from 5% to 20%, see:
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The loading of catalyst (Lewis acid) is usually from 5% to 20%, see:. Chapman C.J., Frost C.G., Hartley J.P., and Whittle A.J. Tetrahedron Lett. 42 (2001) 773
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Chapman, C.J.1
Frost, C.G.2
Hartley, J.P.3
Whittle, A.J.4
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20
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26444457933
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Eklund P.C., Langvik O.K., Waerna J.P., Salmi T.O., Willfoer S.M., and Sjoeholm R.E. Org. Biomol. Chem. 3 (2005) 3336-3347
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Eklund, P.C.1
Langvik, O.K.2
Waerna, J.P.3
Salmi, T.O.4
Willfoer, S.M.5
Sjoeholm, R.E.6
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21
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11844282777
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Min B.-S., Na M.-K., Oh S.-R., Ahn K.-S., Jeong G.-S., Li G., Lee S.-K., Joung H., and Lee H.-K. J. Nat. Prod. 67 (2004) 1980-1984
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Min, B.-S.1
Na, M.-K.2
Oh, S.-R.3
Ahn, K.-S.4
Jeong, G.-S.5
Li, G.6
Lee, S.-K.7
Joung, H.8
Lee, H.-K.9
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30
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1142297395
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Antioxidant activity and phenolic compounds of 112 traditional Chinese medicinal plants associated with anticancer, see:
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Antioxidant activity and phenolic compounds of 112 traditional Chinese medicinal plants associated with anticancer, see:. Cai Y., Luo Q., Sun M., and Corke H. Life Sci. 74 (2004) 2157-2184
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Life Sci.
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Cai, Y.1
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Corke, H.4
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31
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20544439638
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The use of butenolides as natural anti-HIVconstituents, see:
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The use of butenolides as natural anti-HIVconstituents, see:. Planta Medica 71 (2005) 452-457
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32
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33845282438
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Corey E.J., Bakshi R.K., Shibata S., Chen C.-P., and Singh V.K. J. Am. Chem. 109 (1987) 7925
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Corey, E.J.1
Bakshi, R.K.2
Shibata, S.3
Chen, C.-P.4
Singh, V.K.5
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33
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0034694683
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Catalytic enantioselective Friedel-Crafts reactions of aromatic compounds with glyoxylate had been developed by Jorgensen recently, see:
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Catalytic enantioselective Friedel-Crafts reactions of aromatic compounds with glyoxylate had been developed by Jorgensen recently, see:. Gathergood N., Zhuang W., and Jørgensen K.A. J. Am. Chem. Soc. 122 (2000) 12517
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Gathergood, N.1
Zhuang, W.2
Jørgensen, K.A.3
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37
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22244482729
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Zhang J., Das Sarma K., Curran T.T., Belmont D.T., and Davidson J.G. J. Org. Chem. 70 (2005) 5890
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Zhang, J.1
Das Sarma, K.2
Curran, T.T.3
Belmont, D.T.4
Davidson, J.G.5
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38
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0002187048
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3 has been used for demethylation of phenolic methyl ethers, see:
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3 has been used for demethylation of phenolic methyl ethers, see:. Prager R.H., and Tan Y.T. Tetrahedron Lett. 38 (1967) 3661
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Tetrahedron Lett.
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Prager, R.H.1
Tan, Y.T.2
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44
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33847690698
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3, mucochloric acid reacts with toluene giving Friedel-Crafts acylation product in 62% yield. See: J. Pharm. Pharmacol. 2003, 55, 1259-1265.
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45
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33847660070
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note
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4 as catalyst.
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