-
15
-
-
19744366251
-
-
R.A. Sheldon Green Chem. 7 2005 267 and references are therein
-
(2005)
Green Chem.
, vol.7
, pp. 267
-
-
Sheldon, R.A.1
-
20
-
-
0027965797
-
-
M. Yamaguchi, H.J. Park, M. Hirame, K. Torisu, S. Nakamura, T. Minami, H. Nishihara, and T. Hiraoka Bull. Chem. Soc. Jpn. 67 1994 1717
-
(1994)
Bull. Chem. Soc. Jpn.
, vol.67
, pp. 1717
-
-
Yamaguchi, M.1
Park, H.J.2
Hirame, M.3
Torisu, K.4
Nakamura, S.5
Minami, T.6
Nishihara, H.7
Hiraoka, T.8
-
25
-
-
84989592263
-
-
A. De Meijere, S. Kozhushkov, T. Haumann, R. Boese, C. Puls, M.J. Scott, and L.T. Cooney Chem. Eur. J. 1 1995 124
-
(1995)
Chem. Eur. J.
, vol.1
, pp. 124
-
-
De Meijere, A.1
Kozhushkov, S.2
Haumann, T.3
Boese, R.4
Puls, C.5
Scott, M.J.6
Cooney, L.T.7
-
27
-
-
33749419923
-
-
Y.Z. Zhou, H.Y. Ma, H. Chen, L. Qiao, Y. Yao, J.Q. Cao, and Y.H. Pei Chem. Pharm. Bull. 54 2006 1455
-
(2006)
Chem. Pharm. Bull.
, vol.54
, pp. 1455
-
-
Zhou, Y.Z.1
Ma, H.Y.2
Chen, H.3
Qiao, L.4
Yao, Y.5
Cao, J.Q.6
Pei, Y.H.7
-
30
-
-
0035932610
-
-
G. Zeni, R.B. Panatieri, E. Lissner, P.H. Menezes, A.L. Braga, and H.A. Stefani Org. Lett. 3 2001 819
-
(2001)
Org. Lett.
, vol.3
, pp. 819
-
-
Zeni, G.1
Panatieri, R.B.2
Lissner, E.3
Menezes, P.H.4
Braga, A.L.5
Stefani, H.A.6
-
33
-
-
0042197185
-
-
J.S. Yadav, B.V.S. Reddy, K.B. Reddy, K.U. Gayathri, and A.R. Prasad Tetrahedron Lett. 44 2003 6493
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 6493
-
-
Yadav, J.S.1
Reddy, B.V.S.2
Reddy, K.B.3
Gayathri, K.U.4
Prasad, A.R.5
-
38
-
-
14844321851
-
-
Z.S. Hou, N. Theyssen, A. Brindmann, and W. Leitner Angew. Chem., Int. Ed. 44 2005 1346
-
(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 1346
-
-
Hou, Z.S.1
Theyssen, N.2
Brindmann, A.3
Leitner, W.4
-
43
-
-
79957949084
-
-
note
-
3): δ -108.5. (b) The procedure of catalyst recycle: The PEG phase containing the catalyst was separated by adding diethyl ether (15 mL) to the reaction mixture upon the reaction completion and then dried at 60 °C under vacuum. The recovered catalyst was directly used for the next run by supplying frech the substrate and oxygen. The Glaser oxidative homocoupling reaction was performed under identical reaction conditions.
-
-
-
-
56
-
-
28944444950
-
-
S. Chandrasekhar, N.R. Reddy, S.S. Sultana, Ch. Narsihmulu, and K.V. Reddy Tetrahedron 62 2006 338
-
(2006)
Tetrahedron
, vol.62
, pp. 338
-
-
Chandrasekhar, S.1
Reddy, N.R.2
Sultana, S.S.3
Narsihmulu, C.4
Reddy, K.V.5
-
57
-
-
38949138424
-
-
D.-Q. Xu, S.-P. Luo, Y.-F. Wang, A.-B. Xia, H.-D. Yue, L.-P. Wang, and Z.-Y. Xu Chem. Commun. 42 2007 4393
-
(2007)
Chem. Commun.
, vol.42
, pp. 4393
-
-
Xu, D.-Q.1
Luo, S.-P.2
Wang, Y.-F.3
Xia, A.-B.4
Yue, H.-D.5
Wang, L.-P.6
Xu, Z.-Y.7
-
58
-
-
79957957315
-
-
S.-P. Luo, S. Zhang, Y.-F. Wang, A.-B. Xia, G.-C. Zhang, X.-H. Du, and D.-Q. Xu J. Org. Chem. 75 2010 188
-
(2010)
J. Org. Chem.
, vol.75
, pp. 188
-
-
Luo, S.-P.1
Zhang, S.2
Wang, Y.-F.3
Xia, A.-B.4
Zhang, G.-C.5
Du, X.-H.6
Xu, D.-Q.7
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