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2/g [determined in our laboratory by B.E.T. method: Brunauer, S.; Hemmett, P. H.; Teller, E. J. Am. Chem. Soc. 1938, 60, 309]. The catalyst was calcined at 200°C for 10 h to remove the mobile surfacial and interstitial water avoiding the collapse of the laminar structure [Alberti, G.; Costantino, U. Layered Solids and their Intercalation Chemistry. In Comprehensive Supramolecular Chemistry; Alberti, G., Bein, T., Eds.; Pergamon: Oxford, 1996; Vol. 7, pp 1-23].
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2/g [determined in our laboratory by B.E.T. method: Brunauer, S.; Hemmett, P. H.; Teller, E. J. Am. Chem. Soc. 1938, 60, 309]. The catalyst was calcined at 200°C for 10 h to remove the mobile surfacial and interstitial water avoiding the collapse of the laminar structure [Alberti, G.; Costantino, U. Layered Solids and their Intercalation Chemistry. In Comprehensive Supramolecular Chemistry; Alberti, G., Bein, T., Eds.; Pergamon: Oxford, 1996; Vol. 7, pp 1-23].
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2/g [determined in our laboratory by B.E.T. method: Brunauer, S.; Hemmett, P. H.; Teller, E. J. Am. Chem. Soc. 1938, 60, 309]. The catalyst was calcined at 200°C for 10 h to remove the mobile surfacial and interstitial water avoiding the collapse of the laminar structure [Alberti, G.; Costantino, U. Layered Solids and their Intercalation Chemistry. In Comprehensive Supramolecular Chemistry; Alberti, G., Bein, T., Eds.; Pergamon: Oxford, 1996; Vol. 7, pp 1-23].
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0345366818
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note
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Calcined zinc and aluminium oxides were prepared from the corresponding nitrates following the same methodology utilized in the preparation of Zn-Al HT(500) (see ref 4a).
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19
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0016159730
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We did not isolate from our reaction mixtures any dithiocarbamate-amine salts which were previously obtained by carrying out the reaction in acetone or ethanol solution and in the presence of an excess of amine: Foye, W. O.; Speranza, J. P. Eur. J. Med. Chem. 1977, 9, 177. Bazavova, I. M.; Dubenko, R. G.; Shevchenko, L. I.; Pel'Kis, P. S. Ukr. Khim. Zh. 1980, 46, 286 (Chem. Abstr. 1980, 93, 71237p).
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Speranza, J.P.2
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20
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0037569560
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We did not isolate from our reaction mixtures any dithiocarbamate-amine salts which were previously obtained by carrying out the reaction in acetone or ethanol solution and in the presence of an excess of amine: Foye, W. O.; Speranza, J. P. Eur. J. Med. Chem. 1977, 9, 177. Bazavova, I. M.; Dubenko, R. G.; Shevchenko, L. I.; Pel'Kis, P. S. Ukr. Khim. Zh. 1980, 46, 286 (Chem. Abstr. 1980, 93, 71237p).
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Ukr. Khim. Zh.
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Pel'Kis, P.S.4
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21
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0344935429
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We did not isolate from our reaction mixtures any dithiocarbamate-amine salts which were previously obtained by carrying out the reaction in acetone or ethanol solution and in the presence of an excess of amine: Foye, W. O.; Speranza, J. P. Eur. J. Med. Chem. 1977, 9, 177. Bazavova, I. M.; Dubenko, R. G.; Shevchenko, L. I.; Pel'Kis, P. S. Ukr. Khim. Zh. 1980, 46, 286 (Chem. Abstr. 1980, 93, 71237p).
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22
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0008713581
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Nord, F.F.2
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0344073400
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See, for example: Gilsdorf, R. T.; Nord, F. F. J. Org. Chem. 1950, 15, 807. Robbins, J. D.; Neal, J. R. Synth. Commun. 1986, 16, 891. Walter, W.; Bode, K.-D. Angew. Chem., Int. Ed. Engl. 1967, 6, 281.
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Neal, J.R.2
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See, for example: Gilsdorf, R. T.; Nord, F. F. J. Org. Chem. 1950, 15, 807. Robbins, J. D.; Neal, J. R. Synth. Commun. 1986, 16, 891. Walter, W.; Bode, K.-D. Angew. Chem., Int. Ed. Engl. 1967, 6, 281.
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0344504629
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note
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A dramatic drop in the yield of 3a(∼40% yield) was effectively observed by carrying out the model reaction in the presence of sulfur (200 mg).
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30
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0344504627
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note
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Powder Diffraction File cards (a) No. 5-0664 and (b) No. 5-0566, JCPDS, International Center for Diffraction Data, Swarthmore, PA.
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