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Pure Appl. Chem., 1985, Vol. 57, No. 12, pp. 1875-1882

http://dx.doi.org/10.1351/pac198557121875

Complex reducing agents: their applications and their outcome in the field of carbonylations

Paul Caubere

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  • Mongin Florence, Harrison-Marchand Anne: Mixed AggregAte (MAA): A Single Concept for All Dipolar Organometallic Aggregates. 2. Syntheses and Reactivities of Homo/HeteroMAAs. Chem. Rev. 2013, 113, 7563. <http://dx.doi.org/10.1021/cr3002966>
  • Appelt Christian, Slootweg J. Chris, Lammertsma Koop, Uhl Werner: A Phosphorus/Aluminum-Based Frustrated Lewis Pair as an Ion Pair Receptor: Alkali Metal Hydride Adducts and Phase-Transfer Catalysis. Angew. Chem. 2012, 124, 6013. <http://dx.doi.org/10.1002/ange.201201855>
  • Appelt Christian, Slootweg J. Chris, Lammertsma Koop, Uhl Werner: A Phosphorus/Aluminum-Based Frustrated Lewis Pair as an Ion Pair Receptor: Alkali Metal Hydride Adducts and Phase-Transfer Catalysis. Angew. Chem. Int. Ed. 2012, 51, 5911. <http://dx.doi.org/10.1002/anie.201201855>
  • Fort Yves: Lithium hydride containing complex reducing agent: A new and simple activation of commercial lithium hydride. Tetrahetron Lett 1995, 36, 6051. <http://dx.doi.org/10.1016/0040-4039(95)01240-I>
  • Seebach Dieter: Struktur und Reaktivität von Lithiumenolaten, vom Pinakolon zur selektivenC-Alkylierung von Peptiden – Schwierigkeiten und Möglichkeiten durch komplexe Strukturen. Angew Chem 1988, 100, 1685. <http://dx.doi.org/10.1002/ange.19881001206>
  • Seebach Dieter: Structure and Reactivity of Lithium Enolates. From Pinacolone to SelectiveC-Alkylations of Peptides. Difficulties and Opportunities Afforded by Complex Structures. Angew Chem Int Ed Engl 1988, 27, 1624. <http://dx.doi.org/10.1002/anie.198816241>
  • Markó László: Transition metals in organic synthesis: hydroformylation, reduction and oxidation. J Organomet Chem 1988, 343, 399. <http://dx.doi.org/10.1016/0022-328X(88)80177-3>
  • Lourak M., Vanderesse R., Fort Y., Caubere P.: Activation of reducing agents. Sodium hydride containing complex reducing agents 25. A one pot one reagent cross-coupling reaction of aryl halides. Tetrahetron Lett 1988, 29, 545. <http://dx.doi.org/10.1016/S0040-4039(00)80145-8>
  • Feghouli A., Fort Y., Vanderesse R., Caubere P.: Activation of reducing agents. Sodium hydride containing complex reducing agents 28. Stereochemistry of reduction of ketones by complex reducing agents. Tetrahetron Lett 1988, 29, 1379. <http://dx.doi.org/10.1016/S0040-4039(00)80301-9>
  • Vanderesse Régis, Fort Yves, Becker Sandrine, Caubere Paul: Activation of reducing agents. Sodium hydride containing complex reducing agents 22. New coupling reaction with “nickel doped” complex reducing agent. Tetrahetron Lett 1986, 27, 3517. <http://dx.doi.org/10.1016/S0040-4039(00)84838-8>
  • Vanderesse R., Lourak M., Fort Y., Caubere P.: Activation of reducing agents. Sodium hydride containing complex reducing agents 23. Symmetrical coupling of nitrogen-containing heterocyclic halides. Tetrahetron Lett 1986, 27, 5483. <http://dx.doi.org/10.1016/S0040-4039(00)85243-0>
  • Fort Y., Vanderesse R., Caubere P.: Activation of reducing agents. Sodium hydride containing complex reducing agents 24. Beneficial effect of Me3SiCl on the reducing properties of NiCRA. Tetrahetron Lett 1986, 27, 5487. <http://dx.doi.org/10.1016/S0040-4039(00)85244-2>