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1
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0001699424
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For the Pd-catalyzed decarboxylative protonation, see:. Tsuji J., Nisar M., and Shimizu I. J. Org. Chem. 50 (1985) 3416-3417
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Tsuji, J.6
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6
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0011446373
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For the Pd-catalyzed decarboxylative allylation, see:
-
For the Pd-catalyzed decarboxylative allylation, see:. Tsuji J., Yamada T., Minami I., Yuhara M., Nisar M., and Shimizu I. J. Org. Chem. 52 (1987) 2988-2995
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Tsuji, J.1
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33746746528
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Waetzig, S.R.1
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Tunge, J.A.4
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11
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33847660868
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Imao D., Itoi A., Yamazaki A., Shirakura M., Ohtoshi R., Ogata K., Ohmori Y., Ohta T., and Ito Y. J. Org. Chem. 72 (2007) 1652-1658
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Imao, D.1
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Ohtoshi, R.5
Ogata, K.6
Ohmori, Y.7
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27844517990
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Nakamura M., Hajra A., Endo K., and Nakamura E. Angew. Chem., Int. Ed. 44 (2005) 7248-7251
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Nakamura, M.1
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27544451620
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Mohr J.T., Behenna D.C., Harned A.M., and Stoltz B.M. Angew. Chem., Int. Ed. 44 (2005) 6924-6927
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Mohr, J.T.1
Behenna, D.C.2
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14
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50949088404
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For our recent Letters on Pd-catalyzed decarboxylative protonation and allylation, see:
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For our recent Letters on Pd-catalyzed decarboxylative protonation and allylation, see:. Gowrisankar S., Kim K.H., Kim S.H., and Kim J.N. Tetrahedron Lett. 49 (2008) 6241-6244
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Gowrisankar, S.1
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17
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4544297587
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For the 1,5-dicarbonyl moiety-containing natural products, see:
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For the 1,5-dicarbonyl moiety-containing natural products, see:. Fleming K.N., and Taylor R.E. Angew. Chem., Int. Ed. 43 (2004) 1728-1730
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(2004)
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Fleming, K.N.1
Taylor, R.E.2
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24
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2442589745
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For the cyclic 1, 5-dicarbonyl and related compounds, see:
-
For the cyclic 1, 5-dicarbonyl and related compounds, see:. Donnoli M.I., Scafato P., Nardiello M., Casarini D., Giorgio E., and Rosini C. Tetrahedron 60 (2004) 4975-4981
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(2004)
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Donnoli, M.I.1
Scafato, P.2
Nardiello, M.3
Casarini, D.4
Giorgio, E.5
Rosini, C.6
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25
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18744380429
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Superchi S., Nardiello M., Donnoli M.I., Scafato P., Menicagli R., and Rosini C.C. R. Chemie 8 (2005) 867-874
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R. Chemie
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Superchi, S.1
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Scafato, P.4
Menicagli, R.5
Rosini, C.C.6
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31
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11144311928
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For the synthesis of cyclic 1,5-dicarbonyl compounds, see:
-
For the synthesis of cyclic 1,5-dicarbonyl compounds, see:. Shen Z.-L., Ji S.-J., and Loh T.-P. Tetrahedron Lett. 46 (2005) 507-508
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(2005)
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Shen, Z.-L.1
Ji, S.-J.2
Loh, T.-P.3
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38
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19944428573
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Simoni D., Rossi M., Rondanin R., Baruchello R., Grisolia G., Eleopra M., Giovannini R., Bozzoli A., Davalli S., Fabio R.D., and Donati D. Tetrahedron Lett. 46 (2005) 759-762
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Simoni, D.1
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Eleopra, M.6
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Bozzoli, A.8
Davalli, S.9
Fabio, R.D.10
Donati, D.11
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40
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34547634770
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Further examples on Mukaiyama-Michael type reaction, see:
-
Further examples on Mukaiyama-Michael type reaction, see:. Harada T., and Kusukawa T. Synlett (2007) 1823-1835
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(2007)
Synlett
, pp. 1823-1835
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Harada, T.1
Kusukawa, T.2
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44
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55749090628
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Sartori A., Curti C., Battistini L., Burreddu P., Rassu G., Pelosi G., Casiraghi G., and Zanardi F. Tetrahedron 64 (2008) 11697-11705
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(2008)
Tetrahedron
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Sartori, A.1
Curti, C.2
Battistini, L.3
Burreddu, P.4
Rassu, G.5
Pelosi, G.6
Casiraghi, G.7
Zanardi, F.8
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45
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27744501832
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For the synthesis of starting materials by Michael addition, see:
-
For the synthesis of starting materials by Michael addition, see:. Ye W., Xu J., Tan C.-T., and Tan C.-H. Tetrahedron Lett. 46 (2005) 6875-6878
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(2005)
Tetrahedron Lett.
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Ye, W.1
Xu, J.2
Tan, C.-T.3
Tan, C.-H.4
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48
-
-
70350083301
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-
3, 300 MHz) δ 1.45-1.62 (m, 1H), 1.78-1.96 (m, 1H), 2.05-2.65 (m, 8H), 2.14 (s, 3H*0.5), 2.17 (s, 3H*0.5), 5.02-5.17
-
3, 300 MHz) δ 1.53-1.78 (m, 2H), 1.84-2.74
-
-
-
-
49
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-
0030745620
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For the references of known compounds, see:
-
For the references of known compounds, see:. Nara S., Toshima H., and Ichihara A. Tetrahedron 53 (1997) 9509-9524
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(1997)
Tetrahedron
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Nara, S.1
Toshima, H.2
Ichihara, A.3
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54
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0034619645
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Banwell M., Hockless D., Jarrott B., Kelly B., Knill A., Longmore R., and Simpson G. J. Chem. Soc., Perkin Trans 1 (2000) 3555-3558
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Banwell, M.1
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Jarrott, B.3
Kelly, B.4
Knill, A.5
Longmore, R.6
Simpson, G.7
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61
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-
0001709509
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-
An interesting palladium-catalyzed intramolecular redox reaction was reported, see:
-
An interesting palladium-catalyzed intramolecular redox reaction was reported, see:. Hogenauer K., and Mulzer J. Org. Lett. 3 (2001) 1495-1497
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(2001)
Org. Lett.
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Hogenauer, K.1
Mulzer, J.2
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62
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0035833016
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Intermolecular redox reaction between propiophenone and bromobenzene was also reported
-
Intermolecular redox reaction between propiophenone and bromobenzene was also reported,. Terao Y., Kametani Y., Wakui H., Satoh T., Miura M., and Nomura M. Tetrahedron 57 (2001) 5967-5974
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(2001)
Tetrahedron
, vol.57
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Terao, Y.1
Kametani, Y.2
Wakui, H.3
Satoh, T.4
Miura, M.5
Nomura, M.6
-
63
-
-
70350079014
-
-
note
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3CN at refluxing temperature. However, the results were almost the same with those of entry 3 (condition D), unfortunately.
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