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85033741819
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Only recently has the existence of acepentalene 1 in the gas phase been proved and an estimate of its lifetime been obtained. R. Haag, D. Schröder, T. Zywietz, H. Jiao, H. Schwarz, P. von R. Schleyer, A. de Meijere, Angew. Chem. 1996, 108, in press; Angew. Chem. Int. Ed. Engl. 1996, 35, in press.
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85033740727
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in press
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Only recently has the existence of acepentalene 1 in the gas phase been proved and an estimate of its lifetime been obtained. R. Haag, D. Schröder, T. Zywietz, H. Jiao, H. Schwarz, P. von R. Schleyer, A. de Meijere, Angew. Chem. 1996, 108, in press; Angew. Chem. Int. Ed. Engl. 1996, 35, in press.
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b) R. Haag, Dissertation, Universität Göttingen, 1995.
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b) O. Reiser, M. Weber, A. de Meijere, Angew. Chem. 1989, 101, 1071; Angew. Chem. Int. Engl. 1989, 28, 1037;
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b) K. Albrecht, Dissertation, Universität Göttingen, 1992.
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Albrecht, K.1
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22
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85033762197
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note
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2 was added. The mixture was stirred for an additional 24 h at 80°C. After cooling to room temperature the reaction mixture was diluted with 20 ml of acetonitrile, filtered through a bed consisting of Celite, silica gel, sea sand and charcoal. The filtrate was concentrated, and the residue purified by chromatography on silica gel. Correct elemental analysis and/or exact molecular masses (HRMS) were obtained for all new compounds.
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23
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85033758369
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note
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5+].
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30
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0347337480
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c) K. Kirschke, D. Timm, H. Müller, J. Prakt. Chem. 1975, 317, 807.
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0342860728
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MM 2 calculations for compounds 5 and 10 have been performed by H. Michaelsen and R. Haag. The calculated olefinic strain (OS) of 10 (12 kcal/mol) does not preclude it from being an intermediate in this Pd-catalysed coupling reaction. For comparison see: a) W. F. Maier, P. von R. Schleyer, J. Am. Chem. Soc. 1981, 103, 1891;
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Maier, W.F.1
Von Schleyer, P.R.2
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33
-
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85033748730
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note
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quat, C=O). - MS (EI, 70 eV), m/z (%): 176 (100) [M+], 153 (4), 134 (24), 133 (10), 119 (5), 106 (38), 91 (62).
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34
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85033743041
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note
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2. G. Carlens, Diplomarbeit, Universität Göttingen, 1994.
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0000702671
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Reviews: R. F. Heck, Org. React. 1982, 27, 345-365; A. de Meijere, F. E. Meyer, Angew. Chem. 1994, 106, 2473; Angew. Chem. Int. Ed. Engl. 1994, 33, 2379.
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Org. React.
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Heck, R.F.1
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Reviews: R. F. Heck, Org. React. 1982, 27, 345-365; A. de Meijere, F. E. Meyer, Angew. Chem. 1994, 106, 2473; Angew. Chem. Int. Ed. Engl. 1994, 33, 2379.
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De Meijere, A.1
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Reviews: R. F. Heck, Org. React. 1982, 27, 345-365; A. de Meijere, F. E. Meyer, Angew. Chem. 1994, 106, 2473; Angew. Chem. Int. Ed. Engl. 1994, 33, 2379.
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38
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85033756926
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note
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3): δ = 65.9 [C-1(4,7)], 65.8 (C-10), 132.2 [C-2(3,5,6,8,9)], 124.8, 125.7, 128.6, 149.2. - MS (EI, 70 eV), m/z(%): 206 (100) [M+], 191 (20), 128 (39), 115 (13), 102 (8), 91 (57).
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39
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85033733088
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to be published
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A. de. Meijere, C.- H. Lee, B. Bengtson, E. Pohl, R. Herbst-Irmer, Chem. Eur. J., to be published; B. Bengtson, Dissertation, Universität Hamburg, 1986.
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Chem. Eur. J.
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De Meijere, A.1
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85033734793
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Dissertation, Universität Hamburg
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A. de. Meijere, C.- H. Lee, B. Bengtson, E. Pohl, R. Herbst-Irmer, Chem. Eur. J., to be published; B. Bengtson, Dissertation, Universität Hamburg, 1986.
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(1986)
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Bengtson, B.1
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41
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85033733704
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note
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+).
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|