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2
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0000633011
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B.M. Trost, & I. Fleming. Oxford: Pergamon Press
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Heck R.F. Trost B.M., Fleming I. Comprehensive Organic Synthesis. 4:1991;833 Pergamon Press, Oxford.
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Comprehensive Organic Synthesis
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Heck, R.F.1
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7
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0034253330
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Wagner M., Köhler K., Djakovitch L., Weinkauf S., Hagen V., Muhler M. Top. Catal. 13:2000;319.
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(2000)
Top. Catal.
, vol.13
, pp. 319
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Wagner, M.1
Köhler, K.2
Djakovitch, L.3
Weinkauf, S.4
Hagen, V.5
Muhler, M.6
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11
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0036236712
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Dell'Anna M.M., Mastrorilli P., Muscio F., Nobile C.F., Suranna G.P. Eur. J. Inorg. Chem. 2002;1094.
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(2002)
Eur. J. Inorg. Chem.
, pp. 1094
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Dell'Anna, M.M.1
Mastrorilli, P.2
Muscio, F.3
Nobile, C.F.4
Suranna, G.P.5
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13
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0012919181
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2O (74.46 mg) and SAPO-31 (1 g). The suspension was stirred for 10 h at 90°C. The solid (Pd-SAPO-31) was calcined at 550°C for 6 h and then reduced at 400°C under hydrogen flow for 6 h. Ni-SAPO-31 and Cu-SAPO-31 were prepared in a similar manner using the nitrate salts of Ni and Cu, respectively.
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2O (74.46 mg) and SAPO-31 (1 g). The suspension was stirred for 10 h at 90°C. The solid (Pd-SAPO-31) was calcined at 550°C for 6 h and then reduced at 400°C under hydrogen flow for 6 h. Ni-SAPO-31 and Cu-SAPO-31 were prepared in a similar manner using the nitrate salts of Ni and Cu, respectively.
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15
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0012918308
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The Heck reactions were carried out in a glass, round bottom flask (25 ml) fitted with a water-cooled condenser. In a typical reaction, the halobenzene (1 mmol), methyl acrylate (2 mmol), base (1.5 mmol) and catalyst (4 wt% with respect to halobenzene) were taken in 5 g of solvent. The reaction was conducted at 60-120°C under a nitrogen atmosphere. The progress and completion of the reaction was monitored by gas chromatography. The products were identified by GC-MS.
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The Heck reactions were carried out in a glass, round bottom flask (25 ml) fitted with a water-cooled condenser. In a typical reaction, the halobenzene (1 mmol), methyl acrylate (2 mmol), base (1.5 mmol) and catalyst (4 wt% with respect to halobenzene) were taken in 5 g of solvent. The reaction was conducted at 60-120°C under a nitrogen atmosphere. The progress and completion of the reaction was monitored by gas chromatography. The products were identified by GC-MS.
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16
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0036629097
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Velu S., Wang L., Okazaki M., Suzuki K., Tomura S. Micropor. Mesopor. Mater. 54:2002;113.
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(2002)
Micropor. Mesopor. Mater.
, vol.54
, pp. 113
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Velu, S.1
Wang, L.2
Okazaki, M.3
Suzuki, K.4
Tomura, S.5
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17
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0035962514
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Kukovecz A., Kónya Z., Mönter D., Reschetilowski W., Kiricsi L. J. Mol. Struct. 563-564:2001;403.
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(2001)
J. Mol. Struct.
, vol.403
, pp. 563-564
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Kukovecz, A.1
Kónya, Z.2
Mönter, D.3
Reschetilowski, W.4
Kiricsi, L.5
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18
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0037184451
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Choudary B.M., Madhi S., Chowdari N.S., Kantam M.L., Sreedhar B. J. Am. Chem. Soc. 124:2002;14127.
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(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 14127
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Choudary, B.M.1
Madhi, S.2
Chowdari, N.S.3
Kantam, M.L.4
Sreedhar, B.5
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