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33751386638
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(c) Farina, V.; Krishnan, B.; Marshall, D. R.; Roth, G. P. J. Org. Chem. 1993, 58, 5434-5444.
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Farina, V.1
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6
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0000340061
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Addition of copper salts as co-catalysts: (d) Farina, V.; Kapadia, S.; Krishnan, B.; Wang, C.; Liebeskind, L. S. J. Org. Chem. 1994, 59, 5905-5911.
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Farina, V.1
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7
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0028220832
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(e) Ye, J.; Bhatt, R. K.; Falck, J. R. J. Am. Chem. Soc. 1994, 116, 1-5.
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Ye, J.1
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8
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0028894576
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Roshchin, A. I.; Bumagin, N. A.; Beletskaya, I. P. Tetrahedron Lett. 1995, 36, 125-128.
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Roshchin, A.I.1
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9
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0028944048
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Rai, R.; Aubrecht, K. B.; Collum, D. B. Tetrahedron Lett. 1995, 36, 3111-3114.
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Rai, R.1
Aubrecht, K.B.2
Collum, D.B.3
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10
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33751157148
-
-
4Sn derivatives in aqueous THF at 50 °C have been repoted. See, Busacca, C. A.; Swestock, J.; Johnson, R. E.; Bailey, T. R.; Musza, L.; Rodger, C. A. J. Org. Chem. 1994, 59, 7553-7556.
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Busacca, C.A.1
Swestock, J.2
Johnson, R.E.3
Bailey, T.R.4
Musza, L.5
Rodger, C.A.6
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12
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0028823331
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and references therein
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Heck-type C-C coupling with iodonium salts: Kang, S-K.; Jung, K-Y.; Park, C-H.; Jang, S-B. Tetrahedron Lett. 1995, 36, 8047-8050 and references therein.
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Tetrahedron Lett.
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Kang, S.-K.1
Jung, K.-Y.2
Park, C.-H.3
Jang, S.-B.4
-
13
-
-
85030205337
-
-
note
-
3, 400 MHz) δ 7.26(m, 2H), 7.35(m, 3H), 7.53(m, 2H), 7.69(m, 2H).
-
-
-
-
14
-
-
0000051774
-
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Koser, G. F.; Wettach, R. H.; Troup, J. M.; Frenze, B. A. J. Org. Chem. 1976, 41, 3609-3611.
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Koser, G.F.1
Wettach, R.H.2
Troup, J.M.3
Frenze, B.A.4
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15
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0001764402
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Negishi, E.; Luo, F. T.; Frisbee, R.; Matsushita, H. Heterocycles 1982, 18, 117-122.
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Heterocycles
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Negishi, E.1
Luo, F.T.2
Frisbee, R.3
Matsushita, H.4
-
16
-
-
85030202823
-
-
note
-
3), (5 mol %) for 2 h to give 4a in 91, 82, and 68% yield, respectively.
-
-
-
-
18
-
-
37049107422
-
-
and references therein
-
Gallos, J.; Varvoglis, A.; Alcock, N. W. J. Chem. Soc., Perkin Trans. 1 1985, 757-763 and references therein.
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J. Chem. Soc., Perkin Trans. 1
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Gallos, J.1
Varvoglis, A.2
Alcock, N.W.3
-
19
-
-
85030200697
-
-
note
-
2(0.5 mol %) for 30 min, Pd/C(2 mol %) for 2 h gave the coupled product 5a in 55 and 61% yield, respectively.
-
-
-
-
20
-
-
0001103058
-
-
Kikukawa, K.; Ikenaga, K.; Kono, K.; Toritani, K.; Wada, F.; Matsuda, T. J. Organomet. Chem. 1984, 270, 277-282.
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Kikukawa, K.1
Ikenaga, K.2
Kono, K.3
Toritani, K.4
Wada, F.5
Matsuda, T.6
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22
-
-
0343056042
-
-
Polyakov, V. K.; Zaplyuisvechka, Z. P.; Pivovarevich, L. P.; Surov, Y. N.; Tsukerman, S.V. Khim. Geterosikl. Soedin 1976, 1196 (Chem. Abstr. 1980, 92, 180916j).
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(1976)
Khim. Geterosikl. Soedin
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Polyakov, V.K.1
Zaplyuisvechka, Z.P.2
Pivovarevich, L.P.3
Surov, Y.N.4
Tsukerman, S.V.5
-
23
-
-
85030199789
-
-
Polyakov, V. K.; Zaplyuisvechka, Z. P.; Pivovarevich, L. P.; Surov, Y. N.; Tsukerman, S.V. Khim. Geterosikl. Soedin 1976, 1196 (Chem. Abstr. 1980, 92, 180916j).
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(1980)
Chem. Abstr.
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-
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24
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84984311815
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Meng, Q.; Sun, S.; Bu, X.; You, X. Gaodeng Xuexiao Huaxue Xuebo 1988, 9, 856 (Chem. Abstr. 1989, 111, 195045j).
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(1988)
Gaodeng Xuexiao Huaxue Xuebo
, vol.9
, pp. 856
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Meng, Q.1
Sun, S.2
Bu, X.3
You, X.4
-
25
-
-
85030202191
-
-
Meng, Q.; Sun, S.; Bu, X.; You, X. Gaodeng Xuexiao Huaxue Xuebo 1988, 9, 856 (Chem. Abstr. 1989, 111, 195045j).
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(1989)
Chem. Abstr.
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-
-
-
26
-
-
85030205286
-
-
note
-
1,4-Diiodobenzene was recovered (∼10% yield) along with iodobenzene(50%).
-
-
-
-
27
-
-
85033820781
-
-
The ratios of 4-iodophenyl-substituted thiophene 5d and 4-iodophenyl-phenylacetylene 5e can be increased to 4 : 1 and 2 : 1 respectively by utilizing Kitamura's reagent. For Kitamura's reagent, see, Kitamura, T.; Furuki, R.; Nagata, K.; Zheng, L.; Taniguchi, H. Synlett 1993, 193-194.
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(1993)
Synlett
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-
Kitamura, T.1
Furuki, R.2
Nagata, K.3
Zheng, L.4
Taniguchi, H.5
-
28
-
-
85030209550
-
-
note
-
3 we could not detect any 1,4-diiodobenzene formed.
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-
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