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D. Barton, W. D. Ollis and J. F. Stoddart, Pergaman, Oxford
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Baggett, N.1
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J. March, in Advanced Organic Chemistry, Reactions, Mechanism and Structure, Wiley, New York, 4th edn, 1992, pp. 386–387.
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March, J.1
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5
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For representative examples of homogeneous catalysts for etherification of alcohols, see
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For representative examples of homogeneous catalysts for etherification of alcohols, see: S. Kim K. N. Chung S. Yang J. Org. Chem. 1987 52 3917.
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Kim, S.1
Chung, K.N.2
Yang, S.3
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6
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33846074291
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Wiley, New York, 4th edn
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L. Karas and W. J. Piel, in Kirk-Othmer Encyclopedia of Chemical Technology, Wiley, New York, 4th edn, 1992, vol. 9 pp. 860–876.
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Karas, L.1
Piel, W.J.2
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14
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11444258787
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40: Reactions of benzylic or allylic alcohols with primary or secondary alcohols under reflux conditions:, Sn- and Zr-containing silicate molecular sieve: Reaction of benzylic alcohols with primary aliphatic alcohols at 100 °C
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40: Reactions of benzylic or allylic alcohols with primary or secondary alcohols under reflux conditions: H. Firouzabadi N. Iranpoor A. A. Jafari J. Mol. Catal. A: Chem. 2005 227 97. Sn- and Zr-containing silicate molecular sieve: Reaction of benzylic alcohols with primary aliphatic alcohols at 100 °C:.
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Firouzabadi, H.1
Iranpoor, N.2
Jafari, A.A.3
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15
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33846117174
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2: The synthesis of ethers derived from combinations of p-methoxy-benzyl alcohols with aliphatic alcohols at 65 °C and diphenyl methanol with aliphatic alcohols at 120 °C, respectively
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2: The synthesis of ethers derived from combinations of p-methoxy-benzyl alcohols with aliphatic alcohols at 65 °C and diphenyl methanol with aliphatic alcohols at 120 °C, respectively:.
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Angew. Chem., Int. Ed.
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Corma, A.1
Renz, M.2
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23
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85034352991
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4+-mont were Brønsted acid sites in the etherification
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4+-mont were Brønsted acid sites in the etherification.
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25
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85034369161
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4+-mont-catalyzed etherifications, trace amounts of symmetrical ethers from aliphatic alcohols (2) were formed as by-products
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4+-mont-catalyzed etherifications, trace amounts of symmetrical ethers from aliphatic alcohols (2) were formed as by-products.
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26
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85034373171
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The yields of 3m in the etherification of 1h with 2a were as follows: montmorillonite K-10, 36%; p-toluenesulfonic acid, 18%; H-Y, 5%
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The yields of 3m in the etherification of 1h with 2a were as follows: montmorillonite K-10, 36%; p-toluenesulfonic acid, 18%; H-Y, 5%.
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27
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0024648135
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3 desorption temperatures corresponded to stronger acid sites; see the following reference
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3 desorption temperatures corresponded to stronger acid sites; see the following reference: P. Berteau B. Delmon Catal. Today 1989 5 121.
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(1989)
Catal. Today
, vol.5
, pp. 121
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Berteau, P.1
Delmon, B.2
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28
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85034359838
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3 desorption temperatures (25–500 °C)
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3 desorption temperatures (25–500 °C).
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29
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85034313055
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4+-mont(500) See ESI
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4+-mont(500) See ESI.
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