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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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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/hlca.19760590702openalex-snapshot
The Reduction of Some 1, 2‐Epoxides with Lithium Aluminium Hydride. Preliminary Communication
inferredcites →https://doi.org/10.1021/ja00871a017openalex-snapshot
Reduction with Metal Hydrides. IX. Reaction Paths in the Reduction of Epoxides with Lithium Aluminum Hydride and Aluminum Chloride2
inferredcites →https://doi.org/10.1021/ja01008a037openalex-snapshot
The mechanism of mixed hydride reductions. Effects of reagent composition, nature of halogen, and solvating ligand on the mechanism of epoxide reduction
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4530288openalex-extracted
From Elemol to Fragranced Elemoxide: Synthesis, Bioactivity, and Molecular Docking Insights as Tyrosinase Inhibitor
inferred← citeshttps://doi.org/10.1002/9781118778173.ch12openalex-snapshot
A Formal [3+3] Cycloaddition Approach To Natural Product Synthesis
inferred← citeshttps://doi.org/10.1002/chin.198606084openalex-snapshot
ChemInform Abstract: Reductive Conversion of Some Cyclic and Acyclic vic‐Epoxides to Alcohols by Means of Lithium Aluminium Hydride/ Aluminium Trichloride.
inferred← citeshttps://doi.org/10.1002/ejoc.200400567openalex-snapshot
A Formal [3 + 3] Cycloaddition Approach to Natural‐Product Synthesis
inferred← citeshttps://doi.org/10.1002/ejoc.202300111openalex-snapshot
Highly Selective and Practical Iron‐Catalyzed Formal Hydrogenation of Epoxides to Primary Alcohols Using Formic Acid
inferred← citeshttps://doi.org/10.1016/b978-0-08-052349-1.00249-3openalex-snapshot
Reduction of Epoxides
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00831-4openalex-snapshot
8.29 Reduction of Epoxides
inferred← citeshttps://doi.org/10.1016/b978-008096518-5.00003-4openalex-snapshot
Oxiranes and Oxirenes: Monocyclic
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.08.003openalex-snapshot
Synthesis of (−)-elemoxide, a commercially important fragrance compound
inferred← citeshttps://doi.org/10.1016/s0040-4039(02)00551-8openalex-snapshot
The total synthesis of (±)-arisugacin A
inferred← citeshttps://doi.org/10.1016/s0040-4039(02)02094-4openalex-snapshot
The first enantioselective total synthesis of (−)-arisugacin A
inferred← citeshttps://doi.org/10.1016/s0957-4166(98)00141-4openalex-snapshot
An efficient stereocontrolled synthesis of (−)-10-epi-5β,11-dihydroxyeudesmane and (−)-4,10-epi-5β,11-dihydroxyeudesmane
inferred← citeshttps://doi.org/10.1016/s1874-6004(04)80007-8openalex-snapshot
The Total Synthesis of (-)-Arisugacin A.
inferred← citeshttps://doi.org/10.1134/s1070428008020012openalex-snapshot
Methods and mechanisms of epoxy compounds reduction
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