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The mechanism of mixed hydride reductions. Effects of reagent composition, nature of halogen, and solvating ligand on the mechanism of epoxide reduction

https://doi.org/10.1021/ja01008a037
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The Reductive Conversion of Some Cyclic and Acyclic vic‐Epoxides to Alcohols by Means of Lithium Aluminium Hydride/Aluminium Trichloride
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Rearrangement of oximes and hydroxylamines with aluminum reductants
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.01.021openalex-snapshot
Quantum chemical studies on the partial hydrogenolysis of methyl 2,3-O-diphenylmethylene-α-l-rhamnopyranoside
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A convenient reagent for conjugate reduction of substituted enones, LiAlH4-CuI
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Kinetics and Mechanism of Polymerization of n-Butyl Vinyl Ether Initiated by Dichloroalane (AlHCl2): A New Cationic Initiating System
inferred← citeshttps://doi.org/10.1246/bcsj.51.2059openalex-snapshot
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inferred← citeshttps://doi.org/10.1246/bcsj.64.306openalex-snapshot
Conjugate Reduction of 2-Butene-1,4-diones with LiAlH4–SbCl3
inferred← citeshttps://doi.org/10.1246/cl.1976.737openalex-snapshot
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Ring-Expansion Reaction of Oximes with Aluminum Reductants
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