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60
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20744439557
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2-[(Trimethylsilyl)ethynyl]pyridine is susceptible to this type of cycloaddition; see ref. [19c]
-
2-[(Trimethylsilyl)ethynyl]pyridine is susceptible to this type of cycloaddition; see ref. [19c].
-
-
-
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61
-
-
20744454014
-
-
Small amounts of 2-(3-cyanopropyl)- and/or 3-(3-cyanopropyl)cyclopenta[b]pyridines were also obtained
-
Small amounts of 2-(3-cyanopropyl)- and/or 3-(3-cyanopropyl)cyclopenta[b]pyridines were also obtained.
-
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-
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62
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0025181123
-
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a) Prepared following the procedure described in: T. K. Jones, R. A. Reamer, R. Desmond, S. G. Mills, J. Am. Chem. Soc. 1990, 112, 2998;
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Jones, T.K.1
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64
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84985155009
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Prepared following the procedure described in: W. Oppolzer, R. L. Snowden, D. P. Simmons, Helv. Chim. Acta 1981, 64, 2002.
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Helv. Chim. Acta
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Oppolzer, W.1
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0001962182
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a) Prepared following the procedure described in: G. E. Jones, D. A. Hendrick, A. B. Holmes, Org. Synth. 1987, 65, 52;
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0006205498
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b) 2f has been described in: D. J. Kim, K. H. Yoo, S. W. Park, J. Org. Chem. 1992, 57, 2347.
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68
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20744448863
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Using AM1 as implemented in MacSpartan Plus, distributed by Wavefunction (1.1.6 for Power Macintosh), 1996.
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1.1.6 for Power Macintosh
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70
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33751157732
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b) P. J. Stevens, F. J. Delvin, C. F. Chabalowski, M. J. Frisch, J. Phys. Chem. 1994, 98, 11623.
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Stevens, P.J.1
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71
-
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20744456009
-
-
3 rather than for the trimethylsilyl group
-
3 rather than for the trimethylsilyl group.
-
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-
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72
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0001584737
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Our results contrast with the trend observed by other authors (prevalence of steric over electronic factors). Y. Wakatsuki, O. Nomura, K. Kitaura, K. Morokuma, H. Yamazaki, J. Am. Chem. Soc. 1983, 105, 1907.
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0003135858
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TMS is usually located α to the nitrogen: C. Saá, D. D. Crotts, G. Hsu, K. P. C. Vollhardt, Synlett 1994, 487.
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Saá, C.1
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74
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0000692295
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For a recent review on acetylenic coupling, see: P. Siemsen, R. C. Livingston, F. Diederich, Angew. Chem. 2000, 112, 2740;
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Waizumi, N.1
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0006154125
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Prepared in 77% yield following the procedure described in ref. [27]. J. L. Dumont, W. Chodkiewicz, P. Cadiot, Bull. Soc. Chim. Fr. 1967, 2, 588.
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Dumont, J.L.1
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79
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20744456616
-
-
For brevity, calculations were performed on nonannelaled pyridine rings
-
For brevity, calculations were performed on nonannelaled pyridine rings.
-
-
-
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82
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0001087837
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Protodesilylation of a TMS group α to a pyridine nitrogen is a known process: R. S. Brown, H. Slebocka-Tilk, J. M. Buschek, J. G. Ulan, J. Am. Chem. Soc. 1984, 106, 5979.
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Y. Rubin, S. Lin, C. B. Knobler, J. Anthony, A. M. Boldi, F. Diederich, J. Am. Chem. Soc. 1991, 113, 6943.
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84
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0001675903
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I-catalyzed cycloadditions of 1,3,5-triynes to form benzenes: R. Boese, A. J. Matzger, D. L. Mohler, K. P. C. Vollhardt, Angew. Chem. 1995, 107, 1630;
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84970566658
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D. C. Craig, H. A. Goodwin, D. Onggo, Aust. J. Chem. 1988, 41, 1157.
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0000930887
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A. Juris, V. Balzani, P. Belser, A. von Zelewsky, Helv. Chim. Acta 1981, 64, 2175.
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0006202872
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S. Ohba, H. Miyamae, S. Sato, Y. Saito, Acta Crystallogr. Sect. B 1979, 35, 1470.
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Ohba, S.1
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90
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0002321864
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2 complexes, see ref. [14a] and the following: J. Yoo, J.-H. Kim, Y. S. Sohn, Y. Do, Inorg. Chim. Acta 1997, 263, 53.
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0006244246
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S. Kitagawa, M. Munakata, N. Miyaji, Inorg. Chem. 1982, 21, 3842.
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Kitagawa, S.1
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92
-
-
20744455534
-
-
2] complex is also observed
-
2] complex is also observed.
-
-
-
|