![Catalytic reductive ring opening of epoxides enabled by zirconocene and photoredox catalysis - ScienceDirect Catalytic reductive ring opening of epoxides enabled by zirconocene and photoredox catalysis - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S245192942200208X-fx1.jpg)
Catalytic reductive ring opening of epoxides enabled by zirconocene and photoredox catalysis - ScienceDirect
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Synthesis of α-Alkylated Ketones via Selective Epoxide Opening/Alkylation Reactions with Primary Alcohols | Organic Letters
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A New and Efficient Epoxide Ring Opening via Poor Nucleophiles: Indole, p-Nitroaniline, Borane and O-Trimethylsilylhydroxylamine in Lithium Perchlorate
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Catalytic Reduction of Cyclic Ethers with Hydrosilanes - Park - 2019 - Chemistry – An Asian Journal - Wiley Online Library
![This explanation says that there is an inversion in stereochemistry when the reducing agent reduces the epoxide, but the stereochemistry after reduction stays the same. Can anyone explain? : r/OrganicChemistry This explanation says that there is an inversion in stereochemistry when the reducing agent reduces the epoxide, but the stereochemistry after reduction stays the same. Can anyone explain? : r/OrganicChemistry](https://preview.redd.it/this-explanation-says-that-there-is-an-inversion-in-v0-u9haznycy8ja1.png?width=640&crop=smart&auto=webp&s=a7f52c99adcb26589348e00890a1204e2d27cab5)
This explanation says that there is an inversion in stereochemistry when the reducing agent reduces the epoxide, but the stereochemistry after reduction stays the same. Can anyone explain? : r/OrganicChemistry
Clean protocol for deoxygenation of epoxides to alkenes via catalytic hydrogenation using gold - Catalysis Science & Technology (RSC Publishing)
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Catalytic Hydrogenation of Epoxides to Alcohols - Thiyagarajan - 2022 - Chemistry – An Asian Journal - Wiley Online Library
![Epoxides are reduced by treatment with lithium aluminum hydride to yield alcohols. Propose a mechanism for this reaction. | Homework.Study.com Epoxides are reduced by treatment with lithium aluminum hydride to yield alcohols. Propose a mechanism for this reaction. | Homework.Study.com](https://homework.study.com/cimages/multimages/16/screenshot_2022-06-25_at_10.47.32_pm6211904680490769642.png)
Epoxides are reduced by treatment with lithium aluminum hydride to yield alcohols. Propose a mechanism for this reaction. | Homework.Study.com
![Recent applications of Cp 2 TiCl in natural product synthesis - Organic Chemistry Frontiers (RSC Publishing) DOI:10.1039/C3QO00024A Recent applications of Cp 2 TiCl in natural product synthesis - Organic Chemistry Frontiers (RSC Publishing) DOI:10.1039/C3QO00024A](https://pubs.rsc.org/image/article/2014/QO/c3qo00024a/c3qo00024a-s3_hi-res.gif)
Recent applications of Cp 2 TiCl in natural product synthesis - Organic Chemistry Frontiers (RSC Publishing) DOI:10.1039/C3QO00024A
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