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2
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25444498936
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For leading references, see: a
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For leading references, see: (a) J. S. Lee, P. L. Fuchs J. Am. Chem. Soc. 127, 13122 (2005);
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Lee, J.S.1
Fuchs, P.L.2
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4
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33645524524
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For our published work toward the ritterazines, see: a
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For our published work toward the ritterazines, see: (a) D. F. Taber, K. V. Taluskie. J. Org. Chem. 71, 2797 (2006);
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J. Org. Chem
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Taber, D.F.1
Taluskie, K.V.2
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6
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0001089453
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For leading references to PM3, see: J. I. Seeman, J. B. Paine III, H. V. Secor, H. S. Im, E. R. Bernstein. J. Am. Chem. Soc. 114, 5269 (1992).
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For leading references to PM3, see: J. I. Seeman, J. B. Paine III, H. V. Secor, H. S. Im, E. R. Bernstein. J. Am. Chem. Soc. 114, 5269 (1992).
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7
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M. G. Organ, J. T. Cooper, L. R. Rogers, F. Soleymanzadeh, T. Paul. J. Org. Chem. 65, 7959 (2000).
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Organ, M.G.1
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Paul, T.5
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8
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Y. Mori, M. Asai, J.-i. Kawade, H. Furukawa. Tetrahedron 51, 5315 (1995).
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Tetrahedron
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Mori, Y.1
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Furukawa, H.4
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11
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0031955351
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(b) S. K. Taylor, D. DeYoung, L. J. Simons, J. R. Vyvyan, M. A. Wemple, N. K. Wood. Synth. Commun. 28, 1691 (1998).
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Synth. Commun
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Taylor, S.K.1
DeYoung, D.2
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Vyvyan, J.R.4
Wemple, M.A.5
Wood, N.K.6
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12
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34249094574
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In parallel with our work, Shair reached the same conclusion about the relative configuration of the spiro center of the ritterazines: S. T. Phillips, M. D. Shair. J. Am. Chem. Soc. 129, 6589 (2007).
-
In parallel with our work, Shair reached the same conclusion about the relative configuration of the spiro center of the ritterazines: S. T. Phillips, M. D. Shair. J. Am. Chem. Soc. 129, 6589 (2007).
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-
-
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13
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33845184216
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For the development of intramolecular diene cyclozirconation, including computational analysis, see: (a) W. A Nugent, D. F Taber. J. Am. Chem. Soc. 111, 6435 (1989);
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For the development of intramolecular diene cyclozirconation, including computational analysis, see: (a) W. A Nugent, D. F Taber. J. Am. Chem. Soc. 111, 6435 (1989);
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14
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0000098015
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(b) D. F. Taber, J. P. Louey, Y. Wang, W. A. Nugent, D. A. Dixon, R. L. Harlow. J. Am. Chem. Soc. 116, 9457 (1994).
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J. Am. Chem. Soc
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Wang, Y.3
Nugent, W.A.4
Dixon, D.A.5
Harlow, R.L.6
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15
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0000284194
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For the development of Zr-based intramolecular diene cyclocarbonylation, see: a
-
For the development of Zr-based intramolecular diene cyclocarbonylation, see: (a) E. Negishi, S. R. Miller. J. Org. Chem. 54, 6014 (1989);
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Negishi, E.1
Miller, S.R.2
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17
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0034679046
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(c) D. F. Taber, W. Zhang, C. L. Campbell, A. R. Rheingold, C. D. Incarvito. J. Am. Chem. Soc. 122, 4813 (2000).
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(2000)
J. Am. Chem. Soc
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Taber, D.F.1
Zhang, W.2
Campbell, C.L.3
Rheingold, A.R.4
Incarvito, C.D.5
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18
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33751500572
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Both ZINDO and MOPAC were used as implemented on a Tektronix CAChe workstation. For a leading reference to the use of ZINDO for transition-metal calculations, see
-
For a leading reference to the use of ZINDO for transition-metal calculations, see: D. R. Kanis, M. A. Ratner, T. J. Marks, M. C. Zerner. Chem. Mater. 3, 19 (1991). Both ZINDO and MOPAC were used as implemented on a Tektronix CAChe workstation.
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(1991)
Chem. Mater
, vol.3
, pp. 19
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Kanis, D.R.1
Ratner, M.A.2
Marks, T.J.3
Zerner, M.C.4
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21
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0028862733
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(b) J. U. Jeong, S. C. Sutton, S. Kim, P. L. Fuchs. J. Am. Chem. Soc. 117, 10157 (1995).
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J. Am. Chem. Soc
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Jeong, J.U.1
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Kim, S.3
Fuchs, P.L.4
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22
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33846999021
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For an alternative route to pyrazines, see
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For an alternative route to pyrazines, see: D. F. Taber, P. W. DeMatteo, K. V. Taluskie. J. Org. Chem. 72, 1492 (2007).
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(2007)
J. Org. Chem
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Taber, D.F.1
DeMatteo, P.W.2
Taluskie, K.V.3
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23
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33750874090
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For the advantages of KH in paraffin, see
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For the advantages of KH in paraffin, see: D. F. Taber, C. G. Nelson. J. Org. Chem. 71, 8973 (2006).
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J. Org. Chem
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Taber, D.F.1
Nelson, C.G.2
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