-
1
-
-
0001009088
-
-
For recent reviews on their syntheses
-
For recent reviews on their syntheses, A. Krief, Tetrahedron, 1986, 42, 1209.
-
(1986)
Tetrahedron
, vol.42
, pp. 1209
-
-
Krief, A.1
-
4
-
-
84990101454
-
-
TXF (X = P) has also been prepared recently
-
TXF (X = P) has also been prepared recently: N. Maigrot, L. Ricard, C. Charrier, and F. Mathey, Angew. Chem., Int. Ed. Engl., 1988, 27, 950.
-
(1988)
Angew. Chem., Int. Ed. Engl
, vol.27
, pp. 950
-
-
Maigrot, N.1
Ricard, L.2
Charrier, C.3
Mathey, F.4
-
5
-
-
33847576768
-
-
Z. I. Yoshida and T. Sugimoto, Angew. Chem., Int. Ed. Engl., 1988, 27, 1573.
-
(1988)
Angew. Chem., Int. Ed. Engl
, vol.27
, pp. 1573
-
-
Yoshida, Z.I.1
Sugimoto, T.2
-
6
-
-
84943026878
-
-
For recent results, see Proceedings of the International Conference on Science and Technology of Synthetic Metals (ICSM 88), Santa Fe, June 26-July 2 1988, in
-
For recent results, see Proceedings of the International Conference on Science and Technology of Synthetic Metals (ICSM 88), Santa Fe, June 26-July 2 1988, in Synth. Met., 1988, 27, Bl-B576.
-
(1988)
Synth. Met
, vol.27
, pp. Bl-B576
-
-
-
8
-
-
37049073554
-
-
S. Rajeswari, Y. A. Jackson, and M. P. Cava, J. Chem. Soc., Chem. Commun., 1988, 1089.
-
(1988)
J. Chem. Soc., Chem. Commun
, pp. 1089
-
-
Rajeswari, S.1
Jackson, Y.A.2
Cava, M.P.3
-
9
-
-
37049112587
-
-
A. Gorgues, P. Batail, and A. Le Coq, J. Chem. Soc., Chem. Commun., 1983, 405.
-
(1983)
J. Chem. Soc., Chem. Commun
, pp. 405
-
-
Gorgues, A.1
Batail, P.2
Le Coq, A.3
-
11
-
-
0001521391
-
-
A. Gorgues, A. Simon, A. Le Coq, A. Hercouet, and F. Corre, Tetrahedron, 1986, 42, 351.
-
(1986)
Tetrahedron
, vol.42
, pp. 351
-
-
Gorgues, A.1
Simon, A.2
Le Coq, A.3
Hercouet, A.4
Corre, F.5
-
12
-
-
37049074535
-
-
D. Stephan, A. Gorgues, A. Belyasmine, and A. Le Coq, J. Chem. Soc., Chem. Commun., 1988, 263.
-
(1988)
J. Chem. Soc., Chem. Commun
, pp. 263
-
-
Stephan, D.1
Gorgues, A.2
Belyasmine, A.3
Le Coq, A.4
-
13
-
-
0001244459
-
-
This reaction proceeds faster with the ethylene triseleno- than with the trithio-carbonate, as when dimethyl acetylenedicarboxylate is used as the electrophilic alkyne
-
This reaction proceeds faster with the ethylene triseleno- than with the trithio-carbonate, as when dimethyl acetylenedicarboxylate is used as the electrophilic alkyne M. V. Lakshmikantham and M. P. Cava, J. Org. Chem., 1976, 41, 882.
-
(1976)
J. Org. Chem
, vol.41
, pp. 882
-
-
Lakshmikantham, M.V.1
Cava, M.P.2
-
17
-
-
37049112587
-
-
A. Gorgues, P. Batail, and A. Le Coq, J. Chem. Soc., Chem. Commun., 1983, 405.
-
(1983)
J. Chem. Soc., Chem. Commun
, pp. 405
-
-
Gorgues, A.1
Batail, P.2
Le Coq, A.3
-
20
-
-
84943074139
-
-
C. U. Pittman, M. Narita, and Y. F. Liang, J. Org. Chem., 1976, 41, 2865.
-
(1976)
J. Org. Chem
, vol.41
, pp. 2865
-
-
Pittman, C.U.1
Narita, M.2
Liang, Y.F.3
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