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2
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33845374421
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E. Vedejs, T.H. Eberlein, D.J. Mazur, C.K. McClure, D.A. Perry, R. Rugged, E. Schwartz, J.S. Stults, D.L. Varie, R.G. Wilde and S. Wittenberger, J. Org. Chem., 1986, 51, 1556.
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J. Org. Chem
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Vedejs, E.1
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Rugged, R.6
Schwartz, E.7
Stults, J.S.8
Varie, D.L.9
Wilde, R.G.10
Wittenberger, S.11
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3
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37049111555
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C.M. Bladon, I.E.G. Ferguson, G.W. Kirby, A.W. Lochead and D.C. McDougall, J. Chem. Soc, Perkin Trans. 1, 1985, 1541.
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J. Chem. Soc, Perkin Trans
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Bladon, C.M.1
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5
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0001251969
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P. Herczegh, M. Szely and R. Bognar, Tetrahedron Lett., 1986, 27, 1509.
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(1986)
Tetrahedron Lett
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Herczegh, P.1
Szely, M.2
Bognar, R.3
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6
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84985610066
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Inverse electronic demand diels-alder reactions have been reported with hc(S)nme2
-
Inverse electronic demand Diels-Alder reactions have been reported with HC(S)NMe2.: G. Seitz, R. Mohr, W. Overheu, R. Allmann and M. Nagel, Angew. Chem., Int. Ed. Engl., 1984, 23, 890.
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Angew. Chem., Int. Ed. Engl., 1984
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Seitz, G.1
Mohr, R.2
Overheu, W.3
Allmann, R.4
Nagel, M.5
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7
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84943982556
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A. Padwa, B. Harrison, S.S. Murphree and P.E. Yeske, J. Org. Chem., 1989, 54, 4233.
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J. Org. Chem
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Padwa, A.1
Harrison, B.2
Murphree, S.S.3
Yeske, P.E.4
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8
-
-
0040160773
-
-
Other papers dealing with Diels-Alder reaction of electron-deficient thioamides have appeared
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Other papers dealing with Diels-Alder reaction of electron-deficient thioamides have appeared: J.D. Friedrich, J. Org. Chem., 1987, 52, 2442.
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(1987)
J.D. Friedrich, J. Org. Chem
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9
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84943982554
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Y. Taraaru, H. Sakata, M. Kimura, H. Harayama, H. Konishi, K. Fugami and S. Tanaka, J. Chem. Soc., Chem. Commun., 1994, 2365.
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J. Chem. Soc., Chem. Commun
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Taraaru, Y.1
Sakata, H.2
Kimura, M.3
Harayama, H.4
Konishi, H.5
Fugami, K.6
Tanaka, S.7
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10
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0025960689
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I.T. Barnish, C.W.G. Fishwick and D.R. Hill, Tetrahedron Lett., 1991, 32, 405.
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(1991)
Tetrahedron Lett
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Barnish, I.T.1
Fishwick, C.2
Hill, D.R.3
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13
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0000046320
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S.S. shaik, j
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A. Prossand S.S. Shaik, J.Am. Chem. Soc, 1981, 103, 3702.
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(1981)
Am. Chem. Soc
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Prossand, A.1
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16
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84943982817
-
Gaussian 92, revision a, gaussian inc
-
Geometry optimisations were carried out at the HF/6-31 + G(d, p) level of theory, using the GAUSSIAN 92 systems of program: M.J. Frisch, G.W. Trucks, M. Head-Gordon, P.M.W. Gill, M.W. Wong, J.B. Foresman, B.G. Johnson, H.B. Schlegel, M.A. Robb, E.S. Reploge, R. Gomperts, J.L. Andres, K. Raghavachari, J.S. Binkley, C. Gonzalez, R.L. Martin, D.J. Fox, D.J. Defrees, J. Baker, J.J.P. Stewart and J.A. Pople, GAUSSIAN 92, revision A, Gaussian Inc., Pittsburg, 1992.
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(1992)
Geometry Optimisations were Carried out at the HF/6-31 + G(D, P) Level of Theory, Using the GAUSSIAN 92 Systems of Program
-
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Frisch, M.J.1
Trucks, G.W.2
Head-Gordon, M.3
Gill, P.4
Wong, M.W.5
Foresman, J.B.6
Johnson, B.G.7
Schlegel, H.B.8
Robb, M.A.9
Reploge, E.S.10
Gomperts, R.11
Andres, J.L.12
Raghavachari, K.13
Binkley, J.S.14
Gonzalez, C.15
Martin, R.L.16
Fox, D.J.17
Defrees, D.J.18
Baker, J.19
Stewart, J.20
Pople, J.A.21
more..
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17
-
-
84986468715
-
-
Diffuse functions were included in order to treat the lone pair properly: T. Clark, J. Chandrasekhar, G.W. Spitznagel and P.V.R. Schleyer, J. Comput. Chem., 1983, 4, 294.
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(1983)
Diffuse Functions were Included in Order to Treat the Lone Pair Properly
, vol.4
, pp. 294
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Clark, T.1
Chandrasekhar, J.2
Spitznagel, G.W.3
Schleyer, P.4
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19
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0000746735
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L.A. Curtiss, D.J. Pochatko, A.E. Read and F. Weinhold, J. Phys. Chem., 1983, 82, 2679.
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(1983)
J. Phys. Chem
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, pp. 2679
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Curtiss, L.A.1
Pochatko, D.J.2
Read, A.E.3
Weinhold, F.4
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20
-
-
0000703066
-
The ππ s → t vertical excitation energies were computed using the cl-singles (Cis) method. this method, which is not always highly quantitatively predictive, is sufficient for our purpose insofar as relative excitation energies are researched
-
The ππ S → T vertical excitation energies were computed using the Cl-Singles (CIS) method. This method, which is not always highly quantitatively predictive, is sufficient for our purpose insofar as relative excitation energies are researched: J.B. Foresman, M. Head-Gordon, J.A. Pople and M.J. Frisch, J. Phys. Chem., 1992, 96, 135.
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(1992)
J. Phys. Chem
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Foresman, J.B.1
Head-Gordon, M.2
Pople, J.A.3
Frisch, M.J.4
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21
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0001697409
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The same is true for hcsnh2
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The same is true for HCSNH2: M.C. Ou and S.Y. Chu, J. Phys. Chem., 1995, 99, 556.
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(1995)
J. Phys. Chem
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Ou, M.C.1
Chu, S.Y.2
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23
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-
0842339191
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Interestingly, in the case of vinylamine the planar structure has been characterized as a transition structure for nitrogen inversion
-
Interestingly, in the case of vinylamine the planar structure has been characterized as a transition structure for nitrogen inversion: K. Lammersta and B.V. Prasad, J. Am. Chem. Soc, 1994, 116, 642.
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(1994)
J. Am. Chem. Soc
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Lammersta, K.1
Prasad, B.V.2
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24
-
-
0001215174
-
Diels-alder reactions are exothermic processes: For recent calculations
-
see
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Diels-Alder reactions are exothermic processes: for recent calculations see: M.A. McCarrick, Y.D. Wu and K.N. Houk, J. Org. Chem., 1993, 58, 3330.
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(1993)
J. Org. Chem
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McCarrick, M.A.1
Wu, Y.D.2
Houk, K.N.3
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25
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84943982816
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the press
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G. Pfister-Guillouzo, A. Senio, F. Gracian, M. Khalid, J.-L. Ripoll and Y. Vallee, New J. Chem., 1995, in the press.
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(1995)
New J. Chem
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Pfister-Guillouzo, G.1
Senio, A.2
Gracian, F.3
Khalid, M.4
Ripoll, J.-L.5
Vallee, Y.6
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26
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0039239859
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J.C. Stowell, B.M. Ham, M.A. Esslinger and A.J. Duplantier, J. Org. Chem., 1989, 54, 1212.
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J. Org. Chem
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Stowell, J.C.1
Ham, B.M.2
Esslinger, M.A.3
Duplantier, A.J.4
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27
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-
0038976562
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Activation of cyanothioformamides by n-acylation has been already pointed out
-
Activation of cyanothioformamides by N-acylation has been already pointed out: K. Friedrich and M. Zamkanei, Tetrahedron Lett., 1917, 18, 2139.
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(1917)
Tetrahedron Lett
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Friedrich, K.1
Zamkanei, M.2
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