-
5
-
-
33751058166
-
-
Other organometallics were also employed, see for example:
-
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7
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0002709728
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Maede T., Okawara R., Tada H., Yasuda K., and Okawara R. J. Organomet. Chem. 27 (1971) 13-18
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Araki S., Shimizu T., Johar P.S., Jin S.J., and Butsugan Y. J. Org. Chem. 56 (1991) 2538-2542
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14
-
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33751063491
-
-
For leading references to other routes to allylic indium reagents and intermediates see:
-
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16
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0000724545
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Araki S., Hirahsita T., Kamei T., Yamamura H., and Kawai M. Org. Lett. 2 (2000) 847-849
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Araki, S.1
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Anwar U., Grigg R., Rasparini M., Savic V., and Sridharan V. Chem. Commun. (2000) 645-646
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3543005957
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Hirashita T., Kambe S., Tsuji H., Omori H., and Araki S. J. Org. Chem. 69 (2004) 5054-5059
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20
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17844361891
-
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Propargylation/allenylation has also been extensively explored. For leading references see:
-
Propargylation/allenylation has also been extensively explored. For leading references see:. Marshall J.A., and Mulhearn J.J. Org. Lett. 7 (2005) 1593-1596
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For a recent example and leading references see:
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For a recent example and leading references see:. Palmelund A., and Masden R. J. Org. Chem. 70 (2005) 8248-8251
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Nair, V; Ros, S.; Jayan, C. L.; Pillai, B. S; Tetrahedron 60, 1959-1982;
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31544471138
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For a recent example and leading references see:
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For a recent example and leading references see:. Jang T.-S., Ku I.W., Jang M.S., Keum G., Kang S.B., Chung B.Y., and Kim Y. Org. Lett. 8 (2006) 195-198
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Org. Lett.
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Jang, T.-S.1
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See for example:
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51
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For leading references see:
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55
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17744395123
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and references therein
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See Vilaivan T., Winotapan C., Banphavichit V., Shinada T., and Ohfune Y. J. Org. Chem. 70 (2005) 3464-3471 and references therein
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See Vilaivan, T.1
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Araki, S.1
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60
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Reviews:
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Fuji K. Chem. Rev. 93 (1993) 2037-2066
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Allylation:
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Hirayama, L.C.1
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79
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33751049558
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Reviews:
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81
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33751032795
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Jacobsen E.N., Pfaltz A., and Yamamoto H. (Eds), Springer, Heidelberg Chapter 27
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Yanagisawa A. In: Jacobsen E.N., Pfaltz A., and Yamamoto H. (Eds). Comprehensive Asymmetric Catalysis Vol. II (1999), Springer, Heidelberg Chapter 27
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Yanagisawa, A.1
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0001310676
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There is some debate about the exact nature of the allylating agent(s), see:
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There is some debate about the exact nature of the allylating agent(s), see:. Chan T.H., and Yang Y. J. Am. Chem. Soc. 121 (1999) 3228-3229
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Capps S.M., Clarke T.P., Charmant J.P.H., Höppe H.A.F., Lloyd-Jones G.C., Murray M., Peakman T.P., Stentiford R.A., Walsh K.E., and Worthington P.A. Eur. J. Org. Chem. (2000) 963-974
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Worthington, P.A.10
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86
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-
33751035953
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-
note
-
Allyl indium halide reagents (generated from allyl iodide or bromide, using In metal or In(I)I) are reported to add exclusively [1,2]- to enones and enals, see Ref. 7a,b.
-
-
-
-
87
-
-
33751049797
-
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For a mechanistically related process involving indoles, see:
-
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90
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0032580408
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Capps S.M., Lloyd-Jones G.C., Murray M., Peakman T.P., and Walsh K.E. Tetrahedron Lett. 39 (1998) 2853-2856
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Walsh, K.E.5
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91
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-
33751059944
-
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Ongoing mechanistic studies suggest that the second allyl group is delivered intermolecularly from indium: Wall, P. W.; Slaughter, J. L.; Parker, A. J.; Laffan, D.; Lloyd-Jones, G. C. Unpublished.
-
-
-
-
92
-
-
33751054721
-
-
* ratio in the modified reagent-as indeed is suggested (but not ruled out) by the linear nature of the correlation in Figure 1. The identity of the modified reagent(s) is the subject of ongoing study.
-
-
-
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93
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33751027660
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2O volumes, and temperature.
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102
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33751022978
-
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note
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4) without racemisation, see Section 4 for details.
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103
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104
-
-
33751067437
-
-
note
-
It should be noted that in the homoallyl-cyclopropanation reaction the acidic surface of the silica gel plate can induce cyclopropane formation and that TLC analysis must thus be interpreted with caution.
-
-
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