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1
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4043123499
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For reviews, see: a
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For reviews, see: (a) Tietze, L. F.; Ila, H.; Bell, H. P. Chem. Rev. 2004, 104, 3453-3516.
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Tietze, L.F.1
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0003441482
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Tsuji, J, Ed, Wiley: Chichester, U.K
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(b) Palladium Reagents and Catalysis; Tsuji, J., Ed.; Wiley: Chichester, U.K., 1995.
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(1995)
Palladium Reagents and Catalysis
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3
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0037102993
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For examples of intermolecular enantioselective nucleopalladation, see: (a) El-Qisairi, A. K, Qaseer, H. A, Henry, P. M. J. Organomet. Chem. 2002, 656, 168-176
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For examples of intermolecular enantioselective nucleopalladation, see: (a) El-Qisairi, A. K.; Qaseer, H. A.; Henry, P. M. J. Organomet. Chem. 2002, 656, 168-176.
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4
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0000221171
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(b) Itami, K.; Palmgren, A.; Thorarensen, A.; Bäckvall, J.-E. J. Org. Chem. 1998, 63, 6466-6471.
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Itami, K.1
Palmgren, A.2
Thorarensen, A.3
Bäckvall, J.-E.4
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5
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33644933443
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For recent intramolecular examples, see: c
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For recent intramolecular examples, see: (c) Yip, K.-T.; Yang, M.; Law, K.-L.; Zhu, N.-Y.; Yang, D. J. Am. Chem. Soc. 2006, 128, 3130-3131.
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(2006)
J. Am. Chem. Soc
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Yip, K.-T.1
Yang, M.2
Law, K.-L.3
Zhu, N.-Y.4
Yang, D.5
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6
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29344449953
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(d) Trend, R. M.; Ramtohul, Y. K.; Stoltz, B. M. J. Am. Chem. Soc. 2005, 127, 17778-17788.
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(2005)
J. Am. Chem. Soc
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Trend, R.M.1
Ramtohul, Y.K.2
Stoltz, B.M.3
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7
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0030941256
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(e) Uozumi, Y.; Kato, K.; Hayashi, T. J. Am. Chem. Soc. 1997, 119, 5063-5064.
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(1997)
J. Am. Chem. Soc
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Uozumi, Y.1
Kato, K.2
Hayashi, T.3
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9
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26844513781
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For a related example, see
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For a related example, see: Chevrin, C.; Bras, J. L.; Hénin, F.; Muzart, J. Synthesis 2005, 2615-2618.
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(2005)
Synthesis
, pp. 2615-2618
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Chevrin, C.1
Bras, J.L.2
Hénin, F.3
Muzart, J.4
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10
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0027111712
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(a) Bols, M.; Binderup, L.; Hansen, J.; Rasmussen, P. Carbohydr. Res. 1992, 235, 141-149.
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(1992)
Carbohydr. Res
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Bols, M.1
Binderup, L.2
Hansen, J.3
Rasmussen, P.4
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(b) Tanaka, Y.; Graefe, U.; Yazawa, K.; Mikami, Y. J. Antibiot. 1998, 51, 589-591.
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(1998)
J. Antibiot
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Tanaka, Y.1
Graefe, U.2
Yazawa, K.3
Mikami, Y.4
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0000162513
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(c) Takenaka, M.; Watanabe, T.; Sugahara, K.; Harada, Y.; Yoshida, S.; Sugawara, F. Biosci., Biotechnol., Biochem. 1997, 61, 1440-1444.
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Biosci., Biotechnol., Biochem
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Takenaka, M.1
Watanabe, T.2
Sugahara, K.3
Harada, Y.4
Yoshida, S.5
Sugawara, F.6
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13
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0027943195
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(d) Huang, L.; Kashiwada, Y.; Cosentino, L. M.; Fan, S.; Chen, C.-H.; McPhail, A. T.; Fujioka, T.; Mihashi, K.; Lee, K.-H. J. Med. Chem. 1994, 37, 3947-3955.
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J. Med. Chem
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Huang, L.1
Kashiwada, Y.2
Cosentino, L.M.3
Fan, S.4
Chen, C.-H.5
McPhail, A.T.6
Fujioka, T.7
Mihashi, K.8
Lee, K.-H.9
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14
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33947381621
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Catalyst decomposition was observed
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Catalyst decomposition was observed.
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15
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4444357128
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For recent enantioselective reactions utilizing chiral quinoline oxazolines, see: a
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For recent enantioselective reactions utilizing chiral quinoline oxazolines, see: (a) Abrunhosa, I.; Bioton, L.; Gaumount, A.; Gulea, M.; Masson, S. Tetrahedron 2004, 60, 9263.
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(2004)
Tetrahedron
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Abrunhosa, I.1
Bioton, L.2
Gaumount, A.3
Gulea, M.4
Masson, S.5
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0034724942
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(b) Chelucci, G.; Sanna, M.; Gladiali, S. Tetrahedron 2000, 56, 2889.
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(2000)
Tetrahedron
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Chelucci, G.1
Sanna, M.2
Gladiali, S.3
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17
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33749828310
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For a recent review of oxazoline synthetic methods, see
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For a recent review of oxazoline synthetic methods, see: Desimoni, G.; Faita, G.; Jorgensen, K. A. Chem. Rev. 2006, 106, 3561-3651.
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(2006)
Chem. Rev
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Desimoni, G.1
Faita, G.2
Jorgensen, K.A.3
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18
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33947431397
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The absolute configuration of the product was determined by comparison to an independently prepared authentic sample. See Supporting Information for details
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The absolute configuration of the product was determined by comparison to an independently prepared authentic sample. See Supporting Information for details.
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