-
1
-
-
33646770947
-
-
and references cited therein
-
Singh, P.; Paul, K.; Holzer, W. Bioorg. Med. Chem. 2006, 14, 5061, and references cited therein.
-
(2006)
Bioorg. Med. Chem
, vol.14
, pp. 5061
-
-
Singh, P.1
Paul, K.2
Holzer, W.3
-
3
-
-
0542368015
-
-
For general overviews of the chemistry of sydnones see: a
-
For general overviews of the chemistry of sydnones see: (a) Baker, W.; Ollis, W. D. Q. Rev. (London) 1957, 11, 15.
-
(1957)
Q. Rev. (London)
, vol.11
, pp. 15
-
-
Baker, W.1
Ollis, W.D.2
-
5
-
-
36549038697
-
-
Browne, D. L.; Helm, M. D.; Plant, A.; Harrity, J. P. A. Angew. Chem., Int. Ed. 2007, 46, 8656.
-
(2007)
Angew. Chem., Int. Ed
, vol.46
, pp. 8656
-
-
Browne, D.L.1
Helm, M.D.2
Plant, A.3
Harrity, J.P.A.4
-
7
-
-
0031905680
-
-
and references cited therein. As well as being of synthetic interest,3 sydnones have shown biological activity with potential applications as antineoplastic, antibacterial, and antihypertensive agents
-
3 sydnones have shown biological activity with potential applications as antineoplastic, antibacterial, and antihypertensive agents: Turnbull, K.; Gross, K. C.; Hall, T. A. Synth. Commun. 1998, 28, 931, and references cited therein.
-
(1998)
Synth. Commun
, vol.28
, pp. 931
-
-
Turnbull, K.1
Gross, K.C.2
Hall, T.A.3
-
10
-
-
0037677148
-
-
Sonogashira cross couplings have been reported recently: Turnbull, K.; Krein, D. M.; Tullis, S. A. Synth. Commun. 2003, 33, 2209.
-
Sonogashira cross couplings have been reported recently: Turnbull, K.; Krein, D. M.; Tullis, S. A. Synth. Commun. 2003, 33, 2209.
-
-
-
-
12
-
-
3242744475
-
-
Dumitraşcu, F.; Mitan, C. I.; Dumitrescu, D.; Drāghici, C.; Cāproiu, M. T. ARKIVOC 2002, 80.
-
(2002)
ARKIVOC
, pp. 80
-
-
Dumitraşcu, F.1
Mitan, C.I.2
Dumitrescu, D.3
Drāghici, C.4
Cāproiu, M.T.5
-
15
-
-
0036589259
-
-
(b) Hassan, J.; Sevignon, M.; Gozzi, C.; Schulz, E.; Lemaire, M. Chem. Rev. 2002, 102, 1359.
-
(2002)
Chem. Rev
, vol.102
, pp. 1359
-
-
Hassan, J.1
Sevignon, M.2
Gozzi, C.3
Schulz, E.4
Lemaire, M.5
-
18
-
-
58149294098
-
-
2 are acidic and this reaction therefore represents an unusual acid-mediated Suzuki coupling reaction.
-
2 are acidic and this reaction therefore represents an unusual acid-mediated Suzuki coupling reaction.
-
-
-
-
19
-
-
34248385279
-
-
For an overview of the cross-coupling reactions of organotrifluoroborates see
-
For an overview of the cross-coupling reactions of organotrifluoroborates see: Molander, G. A.; Ellis, N. Acc. Chem. Res. 2007, 40, 275.
-
(2007)
Acc. Chem. Res
, vol.40
, pp. 275
-
-
Molander, G.A.1
Ellis, N.2
-
20
-
-
34250797354
-
-
Kantchev, E. A. B.: O'Brien, C. J.; Organ, M. G. Angew. Chem., Int. Ed. 2007, 46, 2768.
-
(2007)
Angew. Chem., Int. Ed
, vol.46
, pp. 2768
-
-
Kantchev, E.A.B.1
O'Brien, C.J.2
Organ, M.G.3
-
21
-
-
58149303359
-
-
It appears that 17 undergoes further cross coupling to 9 at a slower rate than the reaction of 2 and 9.
-
It appears that 17 undergoes further cross coupling to 9 at a slower rate than the reaction of 2 and 9.
-
-
-
|