-
4
-
-
0001425132
-
-
Streitwieser AJr, Hollyhead WB, Pudjaatmake AH, Owens PH, Kruger TL, Rubenstein PA, MacQuarrie RA, Brokaw ML, Chu WKC, Niemeyer HM. J. Am. Chem. Soc. 1971; 93: 5088-5096.
-
(1971)
J. Am. Chem. Soc.
, vol.93
, pp. 5088-5096
-
-
Streitwieser Jr., A.1
Hollyhead, W.B.2
Pudjaatmake, A.H.3
Owens, P.H.4
Kruger, T.L.5
Rubenstein, P.A.6
MacQuarrie, R.A.7
Brokaw, M.L.8
Chu, W.K.C.9
Niemeyer, H.M.10
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6
-
-
11644284712
-
-
Koch HF, Biffinger JC, Mishima M, Mustanir, Lodder G. J. Phys. Org. Chem. 1998; 11: 614-617.
-
(1998)
J. Phys. Org. Chem.
, vol.11
, pp. 614-617
-
-
Koch, H.F.1
Biffinger, J.C.2
Mishima, M.3
Mustanir4
Lodder, G.5
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8
-
-
0001152776
-
-
Streitwieser AJr, Hollyhead WB, Sonnichsen G, Pudjaatmake AH, Chang CJ, Kruger TL. J. Am. Chem. Soc. 1971; 93: 5096-5102.
-
(1971)
J. Am. Chem. Soc.
, vol.93
, pp. 5096-5102
-
-
Streitwieser Jr., A.1
Hollyhead, W.B.2
Sonnichsen, G.3
Pudjaatmake, A.H.4
Chang, C.J.5
Kruger, T.L.6
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9
-
-
33746128145
-
-
note
-
iH, see Table I.
-
-
-
-
10
-
-
33746158285
-
-
note
-
8 uses 3.344 as the exponent in their treatment. We use 3.344 value for our calculations.
-
-
-
-
11
-
-
33746166909
-
-
note
-
D.
-
-
-
-
14
-
-
9844268507
-
-
Koch HF, Lodder G, Koch JG, Bogdan DJ, Brown GH, Carlson CA, Dean AB, Hage R, Han P, Hopman JCP, James LA, Knape PM, Roos EC, Sardina ML, Sawyer RA, Scott BO, Testa CAIII, Wickham SD. J. Am. Chem. Soc. 1997; 119: 9965-9974.
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 9965-9974
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-
Koch, H.F.1
Lodder, G.2
Koch, J.G.3
Bogdan, D.J.4
Brown, G.H.5
Carlson, C.A.6
Dean, A.B.7
Hage, R.8
Han, P.9
Hopman, J.C.P.10
James, L.A.11
Knape, P.M.12
Roos, E.C.13
Sardina, M.L.14
Sawyer, R.A.15
Scott, B.O.16
Testa III, C.A.17
Wickham, S.D.18
-
15
-
-
33746129344
-
-
note
-
3, rates for the deuterium and tritium derivatives are used interchangeably.
-
-
-
-
17
-
-
0026573131
-
-
(b) Fujio M, Nakashima K, Tokunaga E, Tauji Y, Tsuno Y. Tetrahedron Lett. 1991; 33: 345-348.
-
(1991)
Tetrahedron Lett.
, vol.33
, pp. 345-348
-
-
Fujio, M.1
Nakashima, K.2
Tokunaga, E.3
Tauji, Y.4
Tsuno, Y.5
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19
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-
0042468782
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-
Koch HF, Dahlberg DB, Lodder G, Root KS, Touchette NA, Solsky RL, Zuck RM, Wagner LJ, Koch NH, Kuzemko MA. J. Am. Chem. Soc. 1983; 105: 2394-2398.
-
(1983)
J. Am. Chem. Soc.
, vol.105
, pp. 2394-2398
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-
Koch, H.F.1
Dahlberg, D.B.2
Lodder, G.3
Root, K.S.4
Touchette, N.A.5
Solsky, R.L.6
Zuck, R.M.7
Wagner, L.J.8
Koch, N.H.9
Kuzemko, M.A.10
-
20
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-
0036820399
-
-
Koch HF, Pomerantz WC, Ruggles EL, van Laren M, van Roon A-M. Collect. Czech. Chem. Commun. 2002; 67: 1505-1516.
-
(2002)
Collect. Czech. Chem. Commun.
, vol.67
, pp. 1505-1516
-
-
Koch, H.F.1
Pomerantz, W.C.2
Ruggles, E.L.3
Van Laren, M.4
Van Roon, A.-M.5
-
22
-
-
33746120480
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-
A detailed discussion of this can be found in reference 14, pp. 9970-9971
-
A detailed discussion of this can be found in reference 14, pp. 9970-9971.
-
-
-
-
30
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-
33845557580
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-
Koch HF, Koch JG, Donovan DB, Toczko AG, Kielbania AJJr. J. Am. Chem. Soc. 1981; 103: 5417-5423.
-
(1981)
J. Am. Chem. Soc.
, vol.103
, pp. 5417-5423
-
-
Koch, H.F.1
Koch, J.G.2
Donovan, D.B.3
Toczko, A.G.4
Kielbania Jr., A.J.5
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31
-
-
33746169988
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-
At 70°C the rate correction for alkoxide-promoted dehydrofluorinations MeOH [1.0] vs. EtOH [30]
-
At 70°C the rate correction for alkoxide-promoted dehydrofluorinations MeOH [1.0] vs. EtOH [30].
-
-
-
-
32
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-
0000486832
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-
Koch HF, McLennan DJ, Koch JG, Tumas W, Dobson B, Koch NH. J. Am. Chem. Soc. 1982; 105: 1930-1937.
-
(1982)
J. Am. Chem. Soc.
, vol.105
, pp. 1930-1937
-
-
Koch, H.F.1
McLennan, D.J.2
Koch, J.G.3
Tumas, W.4
Dobson, B.5
Koch, N.H.6
-
36
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-
33746153320
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Abstracts 17th IUPAC conference on physical organic chemistry
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Sahnghai, China, August 15-20, 2004. Manuscript submitted to January
-
(b) Mustinar, Matsuoka M, Mishima M. Abstracts 17th IUPAC Conference on Physical Organic Chemistry, Sahnghai, China, August 15-20, 2004. Manuscript submitted to Bull. Chem. Soc. Jpn. January, 2006.
-
(2006)
Bull. Chem. Soc. Jpn.
-
-
Mustinar, M.M.1
Mishima, M.2
-
39
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-
0031949090
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-
Wiedermann J, Heiner T, Mioston G, Prakash GKS, Olah GA. Angew. Chem. Int. Ed. 1998; 37: 820.
-
(1998)
Angew. Chem. Int. Ed.
, vol.37
, pp. 820
-
-
Wiedermann, J.1
Heiner, T.2
Mioston, G.3
Prakash, G.K.S.4
Olah, G.A.5
-
40
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-
33746105058
-
-
note
-
2 as the solvent. We had better luck with toluene, but our yields were never above 50%.
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-
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