-
6
-
-
0038301132
-
-
L. Sydnes Chem. Rev. 2003 103 1133 1150
-
(2003)
Chem. Rev.
, vol.103
, pp. 1133-1150
-
-
Sydnes, L.1
-
10
-
-
22944485617
-
-
S. Ma Chem. Rev. 2005 105 2829 2872
-
(2005)
Chem. Rev.
, vol.105
, pp. 2829-2872
-
-
Ma, S.1
-
28
-
-
84897990302
-
-
Personal communication, March, 28, 2013
-
B. Cazes, Personal communication, March, 28, 2013
-
-
-
Cazes, B.1
-
30
-
-
37049077000
-
-
R. E. Rülke D. Kliphuis C. J. Elsevier J. Fraanje K. Goubitz P. W. N. M. van Leeuwen K. Vrieze J. Chem. Soc., Chem. Commun. 1994 1817 1819
-
(1994)
J. Chem. Soc., Chem. Commun.
, pp. 1817-1819
-
-
Rülke, R.E.1
Kliphuis, D.2
Elsevier, C.J.3
Fraanje, J.4
Goubitz, K.5
Van Leeuwen, P.W.N.M.6
Vrieze, K.7
-
31
-
-
0021522459
-
-
No mechanism has been proposed. A catalytic cycle similar to that with phenol as nucleophilic species could occur, see Scheme 4
-
Y. Inoue Y. Ohtsuka H. Hashimoto Bull. Chem. Soc. Jpn. 1984 57 3345 3346
-
(1984)
Bull. Chem. Soc. Jpn.
, vol.57
, pp. 3345-3346
-
-
Inoue, Y.1
Ohtsuka, Y.2
Hashimoto, H.3
-
35
-
-
0035817276
-
-
Y. Nagumo H. Oguri Y. Shindo S. Sasaki T. Oishi M. Hirama Y. Tomioka M. Mizugaki T. Tsumuraya Bioorg. Med. Chem. Lett. 2001 11 2037 2040
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, pp. 2037-2040
-
-
Nagumo, Y.1
Oguri, H.2
Shindo, Y.3
Sasaki, S.4
Oishi, T.5
Hirama, M.6
Tomioka, Y.7
Mizugaki, M.8
Tsumuraya, T.9
-
37
-
-
0011931581
-
-
S. S. Kinderman R. Doodeman J. W. Van Beijma J. C. Russcher K. C. M. F. Tjen T. M. Kooistra H. Mohaselzadeh J. H. Van Maarseveen H. Hiemstra H. E. Schoemaker F. P. J. T. Rutjes Adv. Synth. Catal. 2002 344 736 748
-
(2002)
Adv. Synth. Catal.
, vol.344
, pp. 736-748
-
-
Kinderman, S.S.1
Doodeman, R.2
Van Beijma, J.W.3
Russcher, J.C.4
Tjen, K.C.M.F.5
Kooistra, T.M.6
Mohaselzadeh, H.7
Van Maarseveen, J.H.8
Hiemstra, H.9
Schoemaker, H.E.10
Rutjes, F.P.J.T.11
-
52
-
-
34848888306
-
-
H.-P. Bi X.-Y. Liu F.-R. Gou L.-N. Guo X.-H. Duan X.-Z. Shu Y.-M. Liang Angew. Chem., Int. Ed. 2007 46 7068 7071
-
(2007)
Angew. Chem., Int. Ed.
, vol.46
, pp. 7068-7071
-
-
Bi, H.-P.1
Liu, X.-Y.2
Gou, F.-R.3
Guo, L.-N.4
Duan, X.-H.5
Shu, X.-Z.6
Liang, Y.-M.7
-
62
-
-
84897978147
-
-
translated from Doklady Akad. Nauk, 2001, 378, 61-63
-
B. A. Trofimov R. N. Kudyakova A. G. Mal'kina V. V. Nosyreva N. A. Kalinina A. I. Albanov Doklady Chem. 2001 378 119 121
-
(2001)
Doklady Chem.
, vol.378
, pp. 119-121
-
-
Trofimov, B.A.1
Kudyakova, R.N.2
Mal'Kina, A.G.3
Nosyreva, V.V.4
Kalinina, N.A.5
Albanov, A.I.6
-
63
-
-
0036410660
-
-
translated from Zhurnal Organicheskoi Khimii, 2002, 38, 1139-1143
-
A. G. Mal'kina R. N. Kudyakova V. V. Nosyreva A. V. Afonin B. A. Trofimov Russ. J. Org. Chem. 2002 38 1088 1092
-
(2002)
Russ. J. Org. Chem.
, vol.38
, pp. 1088-1092
-
-
Mal'Kina, A.G.1
Kudyakova, R.N.2
Nosyreva, V.V.3
Afonin, A.V.4
Trofimov, B.A.5
-
93
-
-
37049084553
-
-
T. Gallagher I. W. Davies S. W. Jones D. Lathbury M. F. Mahon K. C. Molloy R. W. Shaw P. Vernon J. Chem. Soc., Perkin Trans. 1 1992 433 440
-
(1992)
J. Chem. Soc., Perkin Trans. 1
, pp. 433-440
-
-
Gallagher, T.1
Davies, I.W.2
Jones, S.W.3
Lathbury, D.4
Mahon, M.F.5
Molloy, K.C.6
Shaw, R.W.7
Vernon, P.8
-
132
-
-
84897977270
-
-
3567762 A 19710302
-
G. D. Shier, US Pat., 3567762 A 19710302, 1971
-
(1971)
US Pat.
-
-
Shier, G.D.1
-
144
-
-
0032483548
-
-
Experiments using alkynyl halides instead of aryl halides and carried out with this Pd/Ag procedure did not yield the corresponding butenolides in decent yields
-
S. Ma Z. Shi J. Org. Chem. 1998 63 6387 6389
-
(1998)
J. Org. Chem.
, vol.63
, pp. 6387-6389
-
-
Ma, S.1
Shi, Z.2
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