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1
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84955394357
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Yamamoto H. Weinheim: Wiley
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Yamamoto H. Lewis Acids in Organic Synthesis. Vols. 1-2:2000;Wiley, Weinheim
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Lewis Acids in Organic Synthesis
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5
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84985532488
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Organotitanium reagents are possessed of Lewis acidic metal center
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Organotitanium reagents are possessed of Lewis acidic metal center, Reetz M.T., Westermann J., Steinbach R. Angew. Chem., Int. Ed. Engl. 19:1980;900-901
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(1980)
Angew. Chem., Int. Ed. Engl.
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Reetz, M.T.1
Westermann, J.2
Steinbach, R.3
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6
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0003537151
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Organocerium reagents exhibit unique reactivity, A.R. Katritzky, O. Meth-Cohn, & C.W. Rees. London: Academic
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Organocerium reagents exhibit unique reactivity, Imamoto T. Katritzky A.R., Meth-Cohn O., Rees C.W. Lanthanides in Organic Synthesis. 1994;Academic, London
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(1994)
Lanthanides in Organic Synthesis
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Imamoto, T.1
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8
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0346518232
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Hojo M., Harada H., Ito H., Hosomi A. J. Chem. Soc., Chem. Commun. 1997;2077-2078
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(1997)
J. Chem. Soc., Chem. Commun.
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Hojo, M.1
Harada, H.2
Ito, H.3
Hosomi, A.4
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9
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0001884490
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For reviews on manganate reagents, see:
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For reviews on manganate reagents, see: Oshima K. J. Organomet. Chem. 575:1999;1-20
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(1999)
J. Organomet. Chem.
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Oshima, K.1
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11
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0034315937
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Hojo M., Sakuragi R., Murakami Y., Baba Y., Hosomi A. Organometallics. 19:2000;4941-4943
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Organometallics
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Hojo, M.1
Sakuragi, R.2
Murakami, Y.3
Baba, Y.4
Hosomi, A.5
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12
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0000223559
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n-2' and terms 'mono-, di-, and trialkylmanganate' are not clear at present and these are tentatively used. For the structure of tetraethylmanganate, see:
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n-2' and terms 'mono-, di-, and trialkylmanganate' are not clear at present and these are tentatively used. For the structure of tetraethylmanganate, see: Morris R.J., Girolami G.S. Organometallics. 8:1989;1478-1485
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(1989)
Organometallics
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, pp. 1478-1485
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Morris, R.J.1
Girolami, G.S.2
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13
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37049093261
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Andersen R.A., Carmona-Guzman E., Gibson J.F., Wilkinson G. J. Chem. Soc., Dalton Trans. 1976;2204-2211
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(1976)
J. Chem. Soc., Dalton Trans.
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Andersen, R.A.1
Carmona-Guzman, E.2
Gibson, J.F.3
Wilkinson, G.4
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14
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2342475197
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note
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3MnMgBr' are possibly in equilibrium through disproportionation. Such a disproportionation would be the reason why clear difference between these reactions was not observed
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15
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0001299082
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Previously, copper salt was co-used as a catalyst in reactions of organomanganese reagents for conjugate addition to α,β-unsaturated carbonyl compounds and alkylation with alkyl bromides. In these reactions, transmetalation of alkyl group from manganese to copper may possibly be involved. Therefore, these reactions are closely related to copper chemistry
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Previously, copper salt was co-used as a catalyst in reactions of organomanganese reagents for conjugate addition to α, β-unsaturated carbonyl compounds and alkylation with alkyl bromides. In these reactions, transmetalation of alkyl group from manganese to copper may possibly be involved. Therefore, these reactions are closely related to copper chemistry Cahiez G., Alami M. Tetrahedron Lett. 30:1989;3541-3544
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(1989)
Tetrahedron Lett.
, vol.30
, pp. 3541-3544
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Cahiez, G.1
Alami, M.2
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18
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85022900125
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Iron catalyst was also used for synthesis of ketones from acid halides and coupling with vinyl halides
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Cahiez G., Marquais S. Synlett. 1993;45-47. Iron catalyst was also used for synthesis of ketones from acid halides and coupling with vinyl halides
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(1993)
Synlett
, pp. 45-47
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Cahiez, G.1
Marquais, S.2
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21
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2342614235
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note
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4Cl
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