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1
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59249100947
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α-Arylation of carbonyls:
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α-Arylation of carbonyls:
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-
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6
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0000644758
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γ-Arylations of α,β-unsaturated carbonyl compounds:
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Satoh T., Inoh J., Kawamura Y., Kawamura Y., Miura M., and Nomura M. Bull. Chem. Soc. Jpn. 71 (1998) 2239-2246 γ-Arylations of α,β-unsaturated carbonyl compounds:
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(1998)
Bull. Chem. Soc. Jpn.
, vol.71
, pp. 2239-2246
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Satoh, T.1
Inoh, J.2
Kawamura, Y.3
Kawamura, Y.4
Miura, M.5
Nomura, M.6
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9
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59249096548
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Intermolecular arylation at activated benzylic or allylic positions:
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Intermolecular arylation at activated benzylic or allylic positions:
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-
-
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10
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0032565850
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Inoh J., Satoh T., Pivsa-Art S., Miura M., and Nomura M. Tetrahedron Lett. 39 (1998) 4673-4676
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(1998)
Tetrahedron Lett.
, vol.39
, pp. 4673-4676
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Inoh, J.1
Satoh, T.2
Pivsa-Art, S.3
Miura, M.4
Nomura, M.5
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11
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0034665237
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Dyker G., Heiermann J., Miura M., Inoh J., Pivsa-Art S., Satoh T., and Nomura M. Chem.-Eur. J. 6 (2000) 3426-3433
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(2000)
Chem.-Eur. J.
, vol.6
, pp. 3426-3433
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Dyker, G.1
Heiermann, J.2
Miura, M.3
Inoh, J.4
Pivsa-Art, S.5
Satoh, T.6
Nomura, M.7
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17
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59249090326
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Intramolecular arylative cyclization at benzylic positions:
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Intramolecular arylative cyclization at benzylic positions:
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21
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34250781177
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Hu Q.-S. Synlett (2007) 1331-1345
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(2007)
Synlett
, pp. 1331-1345
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Hu, Q.-S.1
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24
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33845207951
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Arylation of N-tert-butylhydrazones as an acyl anion equivalent:
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Arylation of N-tert-butylhydrazones as an acyl anion equivalent:. Takemiya A., and Hartwig J.F. J. Am. Chem. Soc. 128 (2006) 14800-14801
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(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 14800-14801
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Takemiya, A.1
Hartwig, J.F.2
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25
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59249101633
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3)-H arylation involving cleavage of less acidic hydrogens:
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3)-H arylation involving cleavage of less acidic hydrogens:
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30
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33947644069
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Giri R., Maugel N., Li J.-J., Wang D.-H., Breazzano S.P., Saunders L.B., and Yu J.-Q. J. Am. Chem. Soc. 129 (2007) 3510-3511
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(2007)
J. Am. Chem. Soc.
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Giri, R.1
Maugel, N.2
Li, J.-J.3
Wang, D.-H.4
Breazzano, S.P.5
Saunders, L.B.6
Yu, J.-Q.7
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35
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59249095286
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α-Arylation of α-sulfonyl carbonyl compounds:
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α-Arylation of α-sulfonyl carbonyl compounds:
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39
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13744252967
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For α-arylation of methanesulfonamides, see Ref. 6d. Synthesis of benzylic sulfonamides by Pd-catalyzed Negishi coupling of sulfonylmethylzinc chlorides with aryl halides:
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Zeevaart J.G., Parkinson C.J., and de Koning C.B. Tetrahedron Lett. 46 (2005) 1597-1599 For α-arylation of methanesulfonamides, see Ref. 6d. Synthesis of benzylic sulfonamides by Pd-catalyzed Negishi coupling of sulfonylmethylzinc chlorides with aryl halides:
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(2005)
Tetrahedron Lett.
, vol.46
, pp. 1597-1599
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Zeevaart, J.G.1
Parkinson, C.J.2
de Koning, C.B.3
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41
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0344887064
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2Ph was reported to be 23.4 in dimethyl sulfoxide at 25 °C. See:
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2Ph was reported to be 23.4 in dimethyl sulfoxide at 25 °C. See:. Bordwell F.G. Acc. Chem. Res. 1 (1988) 456-463
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(1988)
Acc. Chem. Res.
, vol.1
, pp. 456-463
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Bordwell, F.G.1
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42
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59249091597
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note
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2 was reported to be 22.3 in dimethyl sulfoxide at 25 °C. See Ref. 7.
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43
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59249083393
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note
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The second arylation was observed in direct arylation of phenyl(4-pyridyl)methane providing the corresponding tetraarylmethane. See Ref. 2d.
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-
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44
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0033579627
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Arduengo III A.J., Krafczyk R., Schmutzler R., Craig H.A., Goerlich J.R., Marshall W.J., and Unverzagt M. Tetrahedron 55 (1999) 14523-14534
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(1999)
Tetrahedron
, vol.55
, pp. 14523-14534
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-
Arduengo III, A.J.1
Krafczyk, R.2
Schmutzler, R.3
Craig, H.A.4
Goerlich, J.R.5
Marshall, W.J.6
Unverzagt, M.7
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46
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0037156333
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Diarylmethanesulfonamide skeletons are found in biologically active compounds. See:
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Diarylmethanesulfonamide skeletons are found in biologically active compounds. See:. St-Denis Y., Levesque S., Bachand B., Edmunds J.J., Leblond L., Preville P., Tarazi M., Winocour P.D., and Siddiqui M.A. Bioorg. Med. Chem. Lett. 12 (2002) 1181-1184
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(2002)
Bioorg. Med. Chem. Lett.
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St-Denis, Y.1
Levesque, S.2
Bachand, B.3
Edmunds, J.J.4
Leblond, L.5
Preville, P.6
Tarazi, M.7
Winocour, P.D.8
Siddiqui, M.A.9
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47
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0001573041
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Substitution reactions of sulfones with carbon nucleophiles in the presence of aluminum chloride:
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Substitution reactions of sulfones with carbon nucleophiles in the presence of aluminum chloride:. Brown D.S., Bruno M., Davenport R.J., and Ley S.V. Tetrahedron 45 (1989) 4293-4308
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(1989)
Tetrahedron
, vol.45
, pp. 4293-4308
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Brown, D.S.1
Bruno, M.2
Davenport, R.J.3
Ley, S.V.4
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51
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37049067590
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Gupta B.D., Roy M., Roy S., Kumar M., and Das I. J. Chem. Soc., Perkin Trans. 2 (1990) 537-543
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(1990)
J. Chem. Soc., Perkin Trans. 2
, pp. 537-543
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Gupta, B.D.1
Roy, M.2
Roy, S.3
Kumar, M.4
Das, I.5
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52
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34548336965
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Sun H.-B., Li B., Chen S., Li J., and Hua R. Tetrahedron 63 (2007) 10185-10188
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(2007)
Tetrahedron
, vol.63
, pp. 10185-10188
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-
Sun, H.-B.1
Li, B.2
Chen, S.3
Li, J.4
Hua, R.5
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53
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2942610132
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Yasuda M., Saito T., Ueda M., and Baba A. Angew. Chem., Int. Ed. 43 (2004) 1414-1416
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(2004)
Angew. Chem., Int. Ed.
, vol.43
, pp. 1414-1416
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Yasuda, M.1
Saito, T.2
Ueda, M.3
Baba, A.4
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54
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34147156607
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Yoshida H., Watanabe M., Morishita T., Ohshita J., and Kunai A. Chem. Commun. (2007) 1505-1507
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(2007)
Chem. Commun.
, pp. 1505-1507
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Yoshida, H.1
Watanabe, M.2
Morishita, T.3
Ohshita, J.4
Kunai, A.5
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