1998
DOI: 10.1016/s0040-4039(98)00839-9
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The effect of cosolvent on the reducing power of SmI2 in tetrahydrofuran

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Cited by 109 publications
(60 citation statements)
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“…(2)]. [9] In der Übergangsmetallkatalyse ermöglicht die Verwendung von Lewis-basischen Phosphanen [10] und anderen Liganden [11] die Feinabstimmung von Reaktivität und Stereoselektivität, so bei Kreuzkupplungen [Schema 2, Gl. (3)] [12] und zahllosen anderen Reaktionen.…”
Section: Introductionunclassified
“…(2)]. [9] In der Übergangsmetallkatalyse ermöglicht die Verwendung von Lewis-basischen Phosphanen [10] und anderen Liganden [11] die Feinabstimmung von Reaktivität und Stereoselektivität, so bei Kreuzkupplungen [Schema 2, Gl. (3)] [12] und zahllosen anderen Reaktionen.…”
Section: Introductionunclassified
“…[1Ϫ4] The reduction potential of SmI 2 is in the range of Ϫ1.3 to Ϫ2.2 V, [5] depending on solvents and ligands, which makes SmI 2 particularly useful for selective reduction and various coupling reactions. [6,7] Since SmI 2 has become commercially available, the development of SmI 2 -mediated reactions has rapidly entered different areas of organic synthesis.…”
Section: Introductionmentioning
confidence: 99%
“…While addition of dg to SmI 2 produces a more powerful reductant in comparison to dgme and dgde, its effect is modest in comparison to other additives. [14] To further study the mechanistic impact of coordination on the reactivity of Sm II , the rates of reactions of SmI 2 with benzyl bromide were monitored in the presence of increasing amounts of dg, dgme, and dgde to determine the relationship between the affinity of each ligand for Sm II and the impact on the reactivity of the resulting complex. Benzyl bromide was chosen as a model substrate to simplify the kinetic analysis.…”
mentioning
confidence: 99%