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General discussions: a) R. Noyori. Asymmetric Catalysis in Organic Synthesis, Wiley, New York, 1993, pp. 1-364; b) K. Maruoka, H. Yamamoto in Catalytic Asymmetric Synthesis (Ed.: I. Ojima), VCH, New York, 1993, pp. 413-440; c) K. Mikami in Advances in Catalytic Process (Ed.: M. P. Doyle), JAI, Greenwich, 1995, pp. 1-44.
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General discussions: a) R. Noyori. Asymmetric Catalysis in Organic Synthesis, Wiley, New York, 1993, pp. 1-364; b) K. Maruoka, H. Yamamoto in Catalytic Asymmetric Synthesis (Ed.: I. Ojima), VCH, New York, 1993, pp. 413-440; c) K. Mikami in Advances in Catalytic Process (Ed.: M. P. Doyle), JAI, Greenwich, 1995, pp. 1-44.
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General discussions: a) R. Noyori. Asymmetric Catalysis in Organic Synthesis, Wiley, New York, 1993, pp. 1-364; b) K. Maruoka, H. Yamamoto in Catalytic Asymmetric Synthesis (Ed.: I. Ojima), VCH, New York, 1993, pp. 413-440; c) K. Mikami in Advances in Catalytic Process (Ed.: M. P. Doyle), JAI, Greenwich, 1995, pp. 1-44.
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Comprehensive discussions: a) Y. Yamamoto, N. Asao, Chem. Rev. 1993, 93, 2207-2293; b) D. Hoppe, W. R. Roush, E. J. Thomas in Stereoselective Synthesis, Vol. 3 (Eds.: G. Helmchen, R. W. Hoffmann, J. Mulzer, E. Schaumann), Thieme, Stuttgart, 1996, pp. 1357-1602.
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Comprehensive discussions: a) Y. Yamamoto, N. Asao, Chem. Rev. 1993, 93, 2207-2293; b) D. Hoppe, W. R. Roush, E. J. Thomas in Stereoselective Synthesis, Vol. 3 (Eds.: G. Helmchen, R. W. Hoffmann, J. Mulzer, E. Schaumann), Thieme, Stuttgart, 1996, pp. 1357-1602.
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Reviews: a) W. R. Roush in Comprehensive Organic Synthesis, Vol. 2 (Ed.: C.H. Heathcock), Pergamon, Oxford, 1991, pp. 1-53; b) M. Santell, J.-M. Pons, Lewis Acids and Selectivity in Organic Chemistry, CRC, New York, 1996, pp. 91-184.
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Reviews: a) W. R. Roush in Comprehensive Organic Synthesis, Vol. 2 (Ed.: C.H. Heathcock), Pergamon, Oxford, 1991, pp. 1-53; b) M. Santell, J.-M. Pons, Lewis Acids and Selectivity in Organic Chemistry, CRC, New York, 1996, pp. 91-184.
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a) K. Ishihara, M. Mouri, Q. Gao, T. Maruyama, K. Furuta, H. Yamamoto, J. Am. Chem. Soc. 1993, 115, 11490-11495;
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h) D. R. Gauthier, Jr., E. M. Carreira, Angew. Chem. 1996, 35, 2521-2523; Angew. Chem. Int. Ed. Engl. 1996, 35, 2363-2365;
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Allenyltin compounds are reported (H. Tanaka, A. K. M. Abdul Hai, H. Ogawa, S. Torri, Synlett 1993, 835-836) to be obtained under conditions similar to those we used to obtain propargyltin compounds from 3-substituted propargyl bromides.
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Synlett
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Tanaka, H.1
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IV-promoted reaction was reported; see a) ref. [5c]; b) M. Terada, Y. Matsumoto, Y. Nakamura, K. Mikami, Chem. Commun. 1997, 281-282.
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38
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0001842782
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IV-promoted reaction was reported; see a) ref. [5c]; b) M. Terada, Y. Matsumoto, Y. Nakamura, K. Mikami, Chem. Commun. 1997, 281-282.
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39
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0345140885
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note
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2CuLi at -78°C in THF. Although the literature procedure can be used to prepare regiochemically pure triphenyltin analogues of 4 and 6, it turned out to be unpromising for this purpose mainly because of the lack of reactivity.
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40
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0002313620
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and references therein
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J. A. Marshall, Chem. Rev. 1996, 96, 31-47, and references therein.
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