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Padwa, A.1
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10044237972
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For some related work using this metal-catalyzed domino reaction, see: (a) Hodgson, D. M.; LeStrat, F.; Avery, T. D.; Donohue, A. C.; Brückl, T. J. Org. Chem. 2004, 69, 8796.
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(e) Chiu, P.; Chen, B.; Cheng, K. F. Org. Lett. 2001, 3, 1721.
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(f) Graening, T.; Bette, V.; Neudörfl, J.; Lex, J.; Schmalz, H. G. Org. Lett. 2005, 7, 4317.
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26
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26444541805
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and references therein
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Boger and co-workers have recently described [3+2]-cycloaddition chemistry across the indole π-bond and have elegantly exploited this chemistry for the construction of a variety of aspidosperma alkaloid targets. See: Choi, Y.; Ishikawa, H.; Velcicky, J.; Elliott, G. I.; Miller, M. M.; Boger, D. L. Org. Lett. 2005, 7, 4539 and references therein.
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(b) Regitz, M.; Hocker, J.; Liedhegener, A. Org. Synth. 1973, 5, 179.
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34
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For a review of dealkoxycarbonylations, see: (a) Krapcho, A. P. Synthesis 1982, 805.
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Trost, B. M., Fleming, I., Eds.; Pergamon: Oxford
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Molander, G. A. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon: Oxford, 1991; Vol. 4, pp 251-282.
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Molander, G.A.1
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37
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33750919311
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note
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The authors have deposited coordinates for structure 21 with the Cambridge Crystallographic Data Centre. The coordinates can be obtained on request, from the Director, Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge, B2 1EZ, U.K.
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