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For selected examples of carbometalation of cyclopropenes, see: allylboration: a) Y. N. Bubnov, B. A. Kazanskii, O. A. Nesmeyanova, T. Y. Rudashevskaya, B. M. Mikhailov, Izv. Akad. Nauk SSSR, Ser. Khim. 1977, 2545
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85037298342
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3 carbon of cyclopropenes
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3 carbon of cyclopropenes.
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Recently, Chan et al. claimed that the organoindium reagent generated by the reaction of allyl halides and indium in aqueous media is not allylindium sesquihalide but allylindium(i): T. H. Chan, Y. Yang, J. Am. Chem. Soc. 1999, 121, 3228.
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For example, see: S. Araki, T. Horie, M. Kato, T. Hirashita, H. Yamamura, M. Kawai, Tetrahedron Lett. 1999, 40, 2331.
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85037319802
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Crystallographic data (excluding structure factors) for the structure 3 reported in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication no. CCDC-147767. Copies of the data can be obtained free of charge on application to CCDC, 12 Union Road, Cambridge CB21EZ, UK (fax: (+44)1223-336-033; e-mail: deposit@ccdc.cam.ac.uk)
-
Crystallographic data (excluding structure factors) for the structure 3 reported in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication no. CCDC-147767. Copies of the data can be obtained free of charge on application to CCDC, 12 Union Road, Cambridge CB21EZ, UK (fax: (+44)1223-336-033; e-mail: deposit@ccdc.cam.ac.uk).
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