-
2
-
-
0010392518
-
-
E.-I. Negishi (Ed.), WileyNew York
-
G. Balme, N. Monteiro, D. Bouyssi, in: E.-I. Negishi (Ed.), Handbook of Organopalladium Chemistry for Organic Synthesis, WileyNew York, 2002, pp. 2245-2265
-
(2002)
Handbook of Organopalladium Chemistry for Organic Synthesis
, pp. 2245-2265
-
-
Balme, G.1
Monteiro, N.2
Bouyssi, D.3
-
3
-
-
0037583537
-
-
For reactions involving oxygen nucleophiles see: E.-I. Negishi (Ed.), Wiley, New York
-
For reactions involving oxygen nucleophiles see: S. Cacchi, A. Arcadi, in: E.-I. Negishi (Ed.), Handbook of Organopalladium Chemistry for Organic Synthesis, Wiley, New York, 2002, pp. 2193-2210;
-
(2002)
Handbook of Organopalladium Chemistry for Organic Synthesis
, pp. 2193-2210
-
-
Cacchi, S.1
Arcadi, A.2
-
4
-
-
0037921475
-
-
For reactions involving nitrogen nucleophiles see: (Ed.), Wiley, New York
-
For reactions involving nitrogen nucleophiles see: S. Cacchi, F. Marinelli, E.-I. Negishi (Ed.), Handbook of Organopalladium Chemistry for Organic Synthesis, Wiley, New York, 2002, 2227-2244.
-
(2002)
Handbook of Organopalladium Chemistry for Organic Synthesis
, pp. 2227-2244
-
-
Cacchi, S.1
Marinelli, F.2
Negishi, E.-I.3
-
9
-
-
0142115861
-
-
(Gainesville, FL, United States) [online computer file]
-
C. Bressy, D. Bruyere, D. Bouyssi, G. Balme, ARKIVOC (Gainesville, FL, United States) [online computer file] 5 2002 127
-
(2002)
ARKIVOC
, vol.5
, pp. 127
-
-
Bressy, C.1
Bruyere, D.2
Bouyssi, D.3
Balme, G.4
-
11
-
-
23544472048
-
Asymmetric catalysis of the intermolecular version of this process was however briefly investigated in our laboratories soon after its discovery but with little success
-
PhD dissertation, Lyon
-
N. Monteiro, Asymmetric catalysis of the intermolecular version of this process was however briefly investigated in our laboratories soon after its discovery but with little success, PhD dissertation, Lyon, 1992.
-
(1992)
-
-
Monteiro, N.1
-
16
-
-
0242632859
-
-
E-I. Negishi (Ed.), Wiley, New York
-
M. Shibasaki, F. Miyazaki, in: E-I. Negishi (Ed.), Handbook of Organopalladium Chemistry for Organic Synthesis, Wiley, New York, 2002, 1283-1315;
-
(2002)
Handbook of Organopalladium Chemistry for Organic Synthesis
, pp. 1283-1315
-
-
Shibasaki, M.1
Miyazaki, F.2
-
18
-
-
0344722086
-
-
Unpublished results
-
G. Balme, M. Bottex, D. Bouyssi, T. Lomberget, N. Monteiro, Unpublished results.
-
-
-
Balme, G.1
Bottex, M.2
Bouyssi, D.3
Lomberget, T.4
Monteiro, N.5
-
23
-
-
0028118841
-
-
Examples of Heck reactions involving aryl or vinyltriflates and using dppf, dppb and/or dppp as ligands
-
Examples of Heck reactions involving aryl or vinyltriflates and using dppf, dppb and/or dppp as ligands: S. Laschat, F. Narjes, L.E. Overman, Tetrahedron 50 1994 347
-
(1994)
Tetrahedron
, vol.50
, pp. 347
-
-
Laschat, S.1
Narjes, F.2
Overman, L.E.3
-
24
-
-
0001251141
-
-
W. Cabri., I. Candiani, A. Bedeschi, R. Santi, J. Org. Chem. 57 1992 3558
-
(1992)
J. Org. Chem.
, vol.57
, pp. 3558
-
-
Cabri, W.1
Candiani, I.2
Bedeschi, A.3
Santi, R.4
-
28
-
-
23544440993
-
Preparation of 3-arylbenzofuranones via carbonylation of arylmethylidenecyclohexadienones
-
PCT Int. Appl., WO 9967232 A2 19991229
-
M. Tinkl, S. Evans, P. Nesvadba, Preparation of 3-arylbenzofuranones via carbonylation of arylmethylidenecyclohexadienones, PCT Int. Appl., WO 9967232 A2 19991229 1999
-
(1999)
-
-
Tinkl, M.1
Evans, S.2
Nesvadba, P.3
-
29
-
-
0032568332
-
-
Recently BINAPAs was found to be more effective chiral ligand than BINAP in asymmetric Heck reactions that use aryl triflates, see
-
Recently BINAPAs was found to be more effective chiral ligand than BINAP in asymmetric Heck reactions that use aryl triflates, see: Cho S.Y. Shibasaki M. Tetrahedron Lett. 39 1998 1773
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 1773
-
-
Cho, S.Y.1
Shibasaki, M.2
-
32
-
-
0005515344
-
-
A similar result was recently reported. In this case, either enantiomer of a Heck product was formed using a single enantiomer of the BINAP ligand depending on the presence of tertiary amine or silver salts in the mixture. see
-
A similar result was recently reported. In this case, either enantiomer of a Heck product was formed using a single enantiomer of the BINAP ligand depending on the presence of tertiary amine or silver salts in the mixture. see A. Ashimori, L.E. Overman, J. Org. Chem. 57 1992 4571
-
(1992)
J. Org. Chem.
, vol.57
, pp. 4571
-
-
Ashimori, A.1
Overman, L.E.2
-
33
-
-
0032496952
-
-
A. Ashimori, B. Bachand, L.E. Overman, D.J. Poon, J. Am. Chem. Soc. 120 1998 6477
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 6477
-
-
Ashimori, A.1
Bachand, B.2
Overman, L.E.3
Poon, D.J.4
|