-
3
-
-
0035908267
-
-
c) P. Magnus, D. A. Scott, M. R. Fielding, Tetrahedron Lett. 2001, 42, 4127.
-
(2001)
Tetrahedron Lett
, vol.42
, pp. 4127
-
-
Magnus, P.1
Scott, D.A.2
Fielding, M.R.3
-
4
-
-
0034028158
-
-
B. Jose, M. S. Sulatha, P. M. Pillai, S. Prathapan, Synth. Commun. 2000, 30, 1509.
-
(2000)
Synth. Commun
, vol.30
, pp. 1509
-
-
Jose, B.1
Sulatha, M.S.2
Pillai, P.M.3
Prathapan, S.4
-
5
-
-
0036322382
-
-
N. Iranpoor, H. Firouzabadi, G. Aghapour, Synth. Commun. 2002, 32, 2535.
-
(2002)
Synth. Commun
, vol.32
, pp. 2535
-
-
Iranpoor, N.1
Firouzabadi, H.2
Aghapour, G.3
-
7
-
-
33750298803
-
-
K. Ishihara, Y. Furuya, H. Yamamoto, Angew. Chem. 2002, 114, 3109;
-
(2002)
Angew. Chem
, vol.114
, pp. 3109
-
-
Ishihara, K.1
Furuya, Y.2
Yamamoto, H.3
-
8
-
-
0037119319
-
-
Angew. Chem. Int. Ed. 2002, 41, 2983.
-
(2002)
Chem. Int. Ed
, vol.41
, pp. 2983
-
-
Angew1
-
9
-
-
21044454796
-
-
P. Yan, P. Batamack, G. K. S. Prakash, G. A. Olah, Catal. Lett. 2005, 101, 141.
-
(2005)
Catal. Lett
, vol.101
, pp. 141
-
-
Yan, P.1
Batamack, P.2
Prakash, G.K.S.3
Olah, G.A.4
-
10
-
-
0034335931
-
-
D. C. Barman, A. J. Thakur, D. Prajapati, J. S. Sandhu, Chem. Lett. 2000, 1196.
-
(2000)
Chem. Lett
, pp. 1196
-
-
Barman, D.C.1
Thakur, A.J.2
Prajapati, D.3
Sandhu, J.S.4
-
14
-
-
0013379360
-
-
E. Choi, C. Lee, Y. Na, S. Chang, Org. Lett. 2002, 4, 2369.
-
(2002)
Org. Lett
, vol.4
, pp. 2369
-
-
Choi, E.1
Lee, C.2
Na, Y.3
Chang, S.4
-
16
-
-
14744302558
-
-
B. Thomas, S. Prathapan, S. Sugunan, Microporous Mesoporous Mater. 2005, 79, 21.
-
(2005)
Microporous Mesoporous Mater
, vol.79
, pp. 21
-
-
Thomas, B.1
Prathapan, S.2
Sugunan, S.3
-
17
-
-
0001261252
-
-
H. M. S. Kumar, P. K. Mohanty, M. S. Kumar, J. S. Yadav, Synth. Commun. 1997, 27, 1327.
-
(1997)
Synth. Commun
, vol.27
, pp. 1327
-
-
Kumar, H.M.S.1
Mohanty, P.K.2
Kumar, M.S.3
Yadav, J.S.4
-
19
-
-
34250774434
-
-
Three kinds of W-Sn hydroxide catalysts with different Sn/W molar ratios (0.9, 1.9, and 5.2) were prepared and used for the dehydration of benzaldoxime. The W-Sn hydroxide with the Sn/W molar ratio of 1.9 showed the highest catalytic activity, and the order of reactivity was as follows: Sn/W = 1.9(79) > 5.2(9) > 0.9(7), where the values in the parentheses are the percent conversion of benzaldoxime under the conditions given in Table 1.
-
Three kinds of W-Sn hydroxide catalysts with different Sn/W molar ratios (0.9, 1.9, and 5.2) were prepared and used for the dehydration of benzaldoxime. The W-Sn hydroxide with the Sn/W molar ratio of 1.9 showed the highest catalytic activity, and the order of reactivity was as follows: Sn/W = 1.9(79) > 5.2(9) > 0.9(7), where the values in the parentheses are the percent conversion of benzaldoxime under the conditions given in Table 1.
-
-
-
-
20
-
-
0000656358
-
-
R. A. Sheldon, M. Wallau, I. W. C. E. Arends, U. Schuchardt, Acc. Chem. Res. 1998, 31, 485.
-
(1998)
Acc. Chem. Res
, vol.31
, pp. 485
-
-
Sheldon, R.A.1
Wallau, M.2
Arends, I.W.C.E.3
Schuchardt, U.4
-
21
-
-
1642373806
-
-
and references therein
-
A. Corma, Chem. Rev. 1995, 95, 559, and references therein.
-
(1995)
Chem. Rev
, vol.95
, pp. 559
-
-
Corma, A.1
-
22
-
-
34250707923
-
-
It was confirmed by an IR spectrum of pyridine adsorbed on the W-Sn hydroxide (Figure S2 in the Supporting Information) that the quantities of Lewis and Brønsted acid sites were 0.34 and 0.17 mmol g-1, respectively, and lower than those of zeolites such as H-mordenite and H-Y (Figure S3 in the Supporting Information, 18] The IR spectrum was also recorded after the pretreatment of the W-Sn hydroxide (evacuated at 150°C for 3 h, see the Experimental Section, The acidity of the W-Sn hydroxide became much stronger by the pretreatment; the H0 value of the pretreated sample lay between -5.6 and -8.2. However, the reaction rate of benzaldoxime dehydration with the pretreated catalyst (R, 1.8 mM min-1 under the conditions in Table 1) was lower than that with the as-prepared catalyst 8.7 mM min-1, This result is consistent with the fact that catalysts with strong acidity, such as zeolites and
-
-1). This result is consistent with the fact that catalysts with strong acidity, such as zeolites and solid superacids, are not effective for the present dehydration.
-
-
-
-
25
-
-
33244466121
-
-
c) M. Hino, S. Takasaki, S. Furuta, H. Matsuhashi, K. Arata, Catal. Commun. 2006, 7, 162;
-
(2006)
Catal. Commun
, vol.7
, pp. 162
-
-
Hino, M.1
Takasaki, S.2
Furuta, S.3
Matsuhashi, H.4
Arata, K.5
-
31
-
-
0036215638
-
-
3+ sites) in zeolites (See Table S3 in the Supporting Information) while Das and co-workers have reported that H-Y zeolite was active for the direct synthesis of nitriles from hydroxylamine and aldehydes; see: K. V. N. S. Srinivas, E. B. Reddy, B. Das, Synlett 2002, 625.
-
3+ sites) in zeolites (See Table S3 in the Supporting Information) while Das and co-workers have reported that H-Y zeolite was active for the direct synthesis of nitriles from hydroxylamine and aldehydes; see: K. V. N. S. Srinivas, E. B. Reddy, B. Das, Synlett 2002, 625.
-
-
-
-
32
-
-
84973339075
-
-
82nd ed, Ed, D. R. Lida, CRC Press, Washington DC, sec. 10, p
-
a) G. P. Williams in CRC Handbook of Chemistry and Physics, 82nd ed. (Ed.: D. R. Lida), CRC Press, Washington DC, 2001, sec. 10, p. 200-205;
-
(2001)
CRC Handbook of Chemistry and Physics
, pp. 200-205
-
-
Williams, G.P.1
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