Mild reductive rearrangement of oximes and oxime ethers to secondary amines with hydrosilanes catalyzed by B(C6F5)3 - Organic Chemistry Frontiers (RSC Publishing)
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Oxime ethers as versatile precursors in organic synthesis: a review - RSC Advances (RSC Publishing) DOI:10.1039/C5RA15299B
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The local and natural sources in synthetic methods: the practical synthesis of aryl oximes from aryl aldehydes under catalyst-free conditions in mineral water | SpringerLink
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Use your understanding of organic chemistry to provide the mechanism and the reagents for the three-step transformation that gives the following product (* is the radio labeled carbon 14C). | Homework.Study.com
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Asymmetric Reduction of Oxime Ethers Promoted by Chiral Spiroborate Esters with an O3BN Framework | The Journal of Organic Chemistry
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