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reductions < reductive < redux  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 10.
Ident.Authors (with country if any)Title
002891 (2001) Dai Cheng [États-Unis] ; Shirong Zhu [États-Unis] ; Zhifang Yu [États-Unis] ; Theodore Cohen [États-Unis]ChemInform Abstract: The Magnesium—Ene Cyclization Stereochemically Directed by an Allylic Oxyanionic Group and Its Application to a Highly Stereoselective Synthesis of (.+‐.)‐Matatabiether. Allylmagnesium Compounds by Reductive Magnesiation of Allyl Phenyl Sulfides.
002B32 (1999) Fangping Chen [États-Unis] ; Boguslaw Mudryk [États-Unis] ; Theodore Cohen [États-Unis]ChemInform Abstract: Tandem Reductive Lithiations — Carbanionic Cyclizations Yielding Sulfur Stabilized Cyclopropyl‐ and Cyclobutylcarbinyllithiums.
002C54 (1998) S. Zhu [États-Unis] ; T. Cohen [États-Unis]ChemInform Abstract: The Preparation of Synthetically Useful Carbonyl‐Protected δ‐ and ε‐Lithio Ketones via Reductive Lithiation.
002C65 (1998) V. Kulkarni [États-Unis] ; T. Cohen [États-Unis]ChemInform Abstract: Cumyl Phenyl Sulfide Forms Bicumyl Instead of Cumyllithium Upon Reductive Lithiation. Thiophenoxide as a Leaving Group in Nucleophilic Substitution by SET.
002F15 (1996) A. Studer [États-Unis] ; D. P. Curran [États-Unis]ChemInform Abstract: Reductive Coupling and Reductive Demethoxylation of Aromatic Dimethylacetals with SmI2/Trifluoroacetic Acid, SmI2/BF3×Et2O, or SmI2/H2O.
003041 (1995) T. Cohen [États-Unis] ; B. Zhang [États-Unis] ; J. P. Cherkauskas [États-Unis]ChemInform Abstract: A General Preparative Method for Carbonyl‐Protected γ‐ Lithioketones via Reductive Lithiation. Synthetic Uses of the Bishomoenolate Equivalents.
003350 (1992) B. Mudryk [États-Unis] ; T. Cohen [États-Unis]ChemInform Abstract: Regiochemical Control in the Reductive Cleavage of 2‐Alkylated Oxetanes by Use of Trialkylaluminums. Tertiary Organolithiums with γ‐Oxo Functinality.
003363 (1992) D. W. Mccullough [États-Unis] ; M. Bhupathy [États-Unis] ; E. Piccolino [États-Unis] ; T. Cohen [États-Unis]ChemInform Abstract: Highly Efficient Terpenoid Pheromone Syntheses via Regio‐ and Stereocontrolled Processing of Allyllithiums Generated by Reductive Lithiation of Allyl Phenyl Thioethers.
003442 (1991) B. Mudryk [États-Unis] ; T. Cohen [États-Unis]ChemInform Abstract: Synthetically Useful Dianions via Reductive Lithiation of Tetrahydrofurans by Aromatic Radical Anions.
003458 (1991) T. Cohen [États-Unis] ; M. D. Doubleday [États-Unis]ChemInform Abstract: A Simple Method for Producing Cycloalkenyllithiums from Cycloalkanones via Reductive Lithiation of Enol Phenyl Thioethers.

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