-
1
-
-
0141776494
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-
Walter H. Stockmayer Fellow, 1998-2000
-
Walter H. Stockmayer Fellow, 1998-2000.
-
-
-
-
2
-
-
0038296973
-
-
He, Y.; Junk, C. P.; Cawley, J. J.; Lemal, D. M. J. Am. Chem. Soc. 2003, 125, 5590-5591.
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 5590-5591
-
-
He, Y.1
Junk, C.P.2
Cawley, J.J.3
Lemal, D.M.4
-
3
-
-
0029855074
-
-
Zhang, Y.; Smith, J.; Lemal, D. M. J. Am. Chem. Soc. 1996, 118, 9454.
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 9454
-
-
Zhang, Y.1
Smith, J.2
Lemal, D.M.3
-
4
-
-
0000592590
-
-
and references therein
-
Wiberg, K. B.; Matturro, M. G.; Okarma, P. J.; Jason, M. E.; Dailey, W. P.; Burgmaier, G. J.; Bailey, W. F.; Warner, P. Tetrahedron 1986, 42, 1895 and references therein.
-
(1986)
Tetrahedron
, vol.42
, pp. 1895
-
-
Wiberg, K.B.1
Matturro, M.G.2
Okarma, P.J.3
Jason, M.E.4
Dailey, W.P.5
Burgmaier, G.J.6
Bailey, W.F.7
Warner, P.8
-
5
-
-
0141664624
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-
note
-
zpt); for the corresponding cations, the difference is 10.6 kcal/mol. (Spartan: Hehre, W.; Wavefunction, Inc.: 188401 Von Karman, Suite 370, Irvine, CA 92717.)
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-
-
-
6
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0141553132
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-
note
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There may also be a greater degree of steric hindrance in the transition state of the naphthalene reaction.
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-
-
7
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-
0010772364
-
-
Callander, D. D.; Coe, P. L.; Tatlow, J. C.; Uff, A. J. Tetrahedron 1969, 25, 25. Callander, D. D.; Coe, P. L.; Tatlow, J. C. J. Chem. Soc., Chem. Commun. 1966, 143.
-
(1969)
Tetrahedron
, vol.25
, pp. 25
-
-
Callander, D.D.1
Coe, P.L.2
Tatlow, J.C.3
Uff, A.J.4
-
8
-
-
37049131770
-
-
Callander, D. D.; Coe, P. L.; Tatlow, J. C.; Uff, A. J. Tetrahedron 1969, 25, 25. Callander, D. D.; Coe, P. L.; Tatlow, J. C. J. Chem. Soc., Chem. Commun. 1966, 143.
-
(1966)
J. Chem. Soc., Chem. Commun.
, pp. 143
-
-
Callander, D.D.1
Coe, P.L.2
Tatlow, J.C.3
-
9
-
-
0010033509
-
-
Cookson, R. C.; Dance, J.; Godfrey, M. Tetrahedron 1968, 24, 1529.
-
(1968)
Tetrahedron
, vol.24
, pp. 1529
-
-
Cookson, R.C.1
Dance, J.2
Godfrey, M.3
-
11
-
-
0010549034
-
-
Krespan, C. G.; McKusick, B. C.; Cairns, T. L. J. Am. Chem. Soc. 1961, 83, 3428.
-
(1961)
J. Am. Chem. Soc.
, vol.83
, pp. 3428
-
-
Krespan, C.G.1
McKusick, B.C.2
Cairns, T.L.3
-
12
-
-
0012253767
-
-
Hales, N. J.; Heaney, H.; Hollinshead, J. H.; Singh, P. Org. Synth. 1980, 59, 71.
-
(1980)
Org. Synth.
, vol.59
, pp. 71
-
-
Hales, N.J.1
Heaney, H.2
Hollinshead, J.H.3
Singh, P.4
-
13
-
-
0000308452
-
-
Friedman, L.; Lindow, D. F. J. Am. Chem. Soc. 1968, 90, 2329. Friedman, L. J. Am. Chem. Soc. 1967, 89, 3071. Miller, R. G.; Stiles, M. J. Am. Chem. Soc. 1963, 85, 1798.
-
(1968)
J. Am. Chem. Soc.
, vol.90
, pp. 2329
-
-
Friedman, L.1
Lindow, D.F.2
-
14
-
-
33947333803
-
-
Friedman, L.; Lindow, D. F. J. Am. Chem. Soc. 1968, 90, 2329. Friedman, L. J. Am. Chem. Soc. 1967, 89, 3071. Miller, R. G.; Stiles, M. J. Am. Chem. Soc. 1963, 85, 1798.
-
(1967)
J. Am. Chem. Soc.
, vol.89
, pp. 3071
-
-
Friedman, L.1
-
15
-
-
0001123576
-
-
Friedman, L.; Lindow, D. F. J. Am. Chem. Soc. 1968, 90, 2329. Friedman, L. J. Am. Chem. Soc. 1967, 89, 3071. Miller, R. G.; Stiles, M. J. Am. Chem. Soc. 1963, 85, 1798.
-
(1963)
J. Am. Chem. Soc.
, vol.85
, pp. 1798
-
-
Miller, R.G.1
Stiles, M.2
-
16
-
-
0003503919
-
-
See also ref 10
-
Liu, R. S. H. J. Am. Chem. Soc. 1968, 90, 215. Other products arise from further reaction of the bicyclooctatriene adduct. See also ref 10.
-
(1968)
J. Am. Chem. Soc.
, vol.90
, pp. 215
-
-
Liu, R.S.H.1
-
17
-
-
0000300367
-
-
Ciganek, E. Tetrahedron Lett. 1967, 3321. In a remarkable example of Lewis acid catalysis of a Diels-Alder reaction, the dicyanobicyclooctatriene is obtained in 63% yield at room temperature in the presence of aluminum chloride.
-
(1967)
Tetrahedron Lett.
, pp. 3321
-
-
Ciganek, E.1
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