-
2
-
-
60849083576
-
-
Ryu, I.; Matsubara, H.; Nakamura, H.; Curran, D. P. Chem. Rec. 2008, 8, 351
-
(2008)
Chem. Rec.
, vol.8
, pp. 351
-
-
Ryu, I.1
Matsubara, H.2
Nakamura, H.3
Curran, D.P.4
-
5
-
-
0037032214
-
-
Ryu, I.; Matsubara, H.; Yasuda, S.; Nakamura, H.; Curran, D. P. J. Am. Chem. Soc. 2002, 124, 12946
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 12946
-
-
Ryu, I.1
Matsubara, H.2
Yasuda, S.3
Nakamura, H.4
Curran, D.P.5
-
6
-
-
0141629302
-
-
Nakamura, H.; Usui, T.; Kuroda, H.; Ryu, I.; Matsubara, H.; Yasuda, S.; Curran, D. P. Org. Lett. 2003, 5, 1167
-
(2003)
Org. Lett.
, vol.5
, pp. 1167
-
-
Nakamura, H.1
Usui, T.2
Kuroda, H.3
Ryu, I.4
Matsubara, H.5
Yasuda, S.6
Curran, D.P.7
-
8
-
-
27444440161
-
-
Rahman, Md. T.; Kamata, N.; Matsubara, H.; Ryu, I. Synlett 2005, 2664
-
(2005)
Synlett
, pp. 2664
-
-
Rahman, Md.T.1
Kamata, N.2
Matsubara, H.3
Ryu, I.4
-
9
-
-
52149124889
-
-
Matsubara, H.; Tsukida, M.; Yasuda, S.; Ryu, I. J. Fluorine Chem. 2008, 129, 951
-
(2008)
J. Fluorine Chem.
, vol.129
, pp. 951
-
-
Matsubara, H.1
Tsukida, M.2
Yasuda, S.3
Ryu, I.4
-
10
-
-
77955342116
-
-
Matsubara, H.; Tsukida, M.; Ishihara, D.; Kuniyoshi, K.; Ryu, I. Synlett 2010, 2014
-
(2010)
Synlett
, pp. 2014
-
-
Matsubara, H.1
Tsukida, M.2
Ishihara, D.3
Kuniyoshi, K.4
Ryu, I.5
-
14
-
-
31144469485
-
-
Podgoršek, A.; Stavber, S.; Zupan, M.; Iskra, J. Eur. J. Org. Chem. 2006, 483
-
(2006)
Eur. J. Org. Chem.
, pp. 483
-
-
Podgoršek, A.1
Stavber, S.2
Zupan, M.3
Iskra, J.4
-
17
-
-
61349193086
-
-
Ma, K.; Li, S.; Weiss, R. G. Org. Lett. 2008, 10, 4155
-
(2008)
Org. Lett.
, vol.10
, pp. 4155
-
-
Ma, K.1
Li, S.2
Weiss, R.G.3
-
20
-
-
84888138315
-
-
Tojino, M.; Hirose, Y.; Mizuno, M. Tetrahedron Lett. 2013, 54, 7124
-
(2013)
Tetrahedron Lett.
, vol.54
, pp. 7124
-
-
Tojino, M.1
Hirose, Y.2
Mizuno, M.3
-
21
-
-
84929636275
-
-
note
-
Galden HT135 and HT200 are polyether-type perfluorinated solvents, which are commercially available from Solvay Solexis Inc. The kinetic viscosities of Galden HT135 and HT200 at 25°C are 1.0 and 2.4 cSt, respectively.
-
-
-
-
25
-
-
84894127968
-
-
Trotuş, I. T.; Zimmermann, T.; Schüth, F. Chem. Rev. 2014, 114, 1761
-
(2014)
Chem. Rev.
, vol.114
, pp. 1761
-
-
Trotuş, I.T.1
Zimmermann, T.2
Schüth, F.3
-
27
-
-
84929612951
-
-
Paquette, L. A.; Crich, D.; Fuchs, P. L.; Molander, G. A., Eds.; John Wiley & Sons: Chichester, UK
-
Arrington, K. L. In Encyclopedia of Reagents for Organic Synthesis, 2nd ed.; Paquette, L. A.; Crich, D.; Fuchs, P. L.; Molander, G. A., Eds.; John Wiley & Sons: Chichester, UK, 2009; Vol. 1, p 97.
-
(2009)
Encyclopedia of Reagents for Organic Synthesis, 2nd ed.
, vol.1
, pp. 97
-
-
Arrington, K.L.1
-
29
-
-
9644285669
-
-
Sonogashira, K.; Tohda, Y.; Hagihara, N. Tetrahedron Lett. 1975, 16, 4467
-
(1975)
Tetrahedron Lett.
, vol.16
, pp. 4467
-
-
Sonogashira, K.1
Tohda, Y.2
Hagihara, N.3
-
31
-
-
84929636277
-
-
note
-
When this procedure was omitted, the evolution of acetylene was not efficient, resulting in slightly (<5%) lower yields.
-
-
-
-
34
-
-
67649411643
-
-
Wu, L. Y.; Xie, Y. X.; Chen, Z. S.; Niu, Y. N.; Liang, Y. M. Synlett 2009, 1453
-
(2009)
Synlett
, pp. 1453
-
-
Wu, L.Y.1
Xie, Y.X.2
Chen, Z.S.3
Niu, Y.N.4
Liang, Y.M.5
-
35
-
-
78049366114
-
-
Gonda, Z.; Lo{combining double acute accent}rincz, K.; Novák, Z. Tetrahedron Lett. 2010, 51, 6275
-
(2010)
Tetrahedron Lett.
, vol.51
, pp. 6275
-
-
Gonda, Z.1
Lorincz, K.2
Novák, Z.3
-
37
-
-
84860470639
-
-
Peshkov, V. A.; Pereshivko, O. P.; Van der Eycken, E. V. Chem. Soc. Rev. 2012, 41, 3790
-
(2012)
Chem. Soc. Rev.
, vol.41
, pp. 3790
-
-
Peshkov, V.A.1
Pereshivko, O.P.2
Van Der Eycken, E.V.3
-
38
-
-
53849085515
-
-
Patil, M. K.; Keller, M.; Reddy, B. M.; Pale, P.; Sommer, J. Eur. J. Org. Chem. 2008, 4440
-
(2008)
Eur. J. Org. Chem.
, pp. 4440
-
-
Patil, M.K.1
Keller, M.2
Reddy, B.M.3
Pale, P.4
Sommer, J.5
-
41
-
-
66249139213
-
-
Zhang, Y.; Li, P.; Wang, M.; Wang, L. J. Org. Chem. 2009, 74, 4364
-
(2009)
J. Org. Chem.
, vol.74
, pp. 4364
-
-
Zhang, Y.1
Li, P.2
Wang, M.3
Wang, L.4
-
42
-
-
8444238805
-
-
Gommermann, N.; Koradin, C.; Polborn, K.; Knochel, P. Angew. Chem. 2003, 115, 5941
-
(2003)
Angew. Chem.
, vol.115
, pp. 5941
-
-
Gommermann, N.1
Koradin, C.2
Polborn, K.3
Knochel, P.4
-
44
-
-
17144402882
-
-
Knöpfel, T. F.; Aschwanden, P.; Ichikawa, T.; Watanabe, T.; Carreira, E. M. Angew. Chem. 2004, 116, 6097
-
(2004)
Angew. Chem.
, vol.116
, pp. 6097
-
-
Knöpfel, T.F.1
Aschwanden, P.2
Ichikawa, T.3
Watanabe, T.4
Carreira, E.M.5
-
46
-
-
84859355181
-
-
Lin, Z.; Yu, D.; Sum, Y. N.; Zhang, Y. ChemSusChem 2012, 5, 625
-
(2012)
ChemSusChem
, vol.5
, pp. 625
-
-
Lin, Z.1
Yu, D.2
Sum, Y.N.3
Zhang, Y.4
-
47
-
-
84929636278
-
-
note
-
No oxidative coupling products of the alkynes were observed.
-
-
-
-
48
-
-
84929636279
-
-
note
-
A significant decrease of isolated yields was caused by the difficulty in the separation of unreacted substrates from the products.
-
-
-
-
49
-
-
84929636280
-
-
note
-
To examine the scalability of the PV system with acetylene gas evolution, Sonogashira coupling with 4.08 g (20 mmol) of iodobenzene was carried out in a larger test tube (30 mm φ x 150 mm) to afford diphenylacetylene in 78% yield, indicating that the Sonogashira reaction can be safely performed at the gram scale using the PV method.
-
-
-
|