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Reactions of amines. XVIII. Oxidative rearrangement of amides with lead tetraacetate

https://doi.org/10.1021/jo00912a019
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inferred← citeshttps://doi.org/10.2139/ssrn.4496949openalex-extracted
inferred← citeshttps://doi.org/10.1002/047084289x.rl006openalex-snapshot
Lead(IV) Acetate
inferred← citeshttps://doi.org/10.1002/047084289x.rl006.pub2openalex-snapshot
Lead(IV) Acetate
inferred← citeshttps://doi.org/10.1002/0471264180.os078.26openalex-snapshot
Methyl Carbamate Formation Via Modified H ofmann Rearrangement Reactions: Methyl N‐(p‐Methoxyphenyl)Carbamate
inferred← citeshttps://doi.org/10.1002/9780470186770.refsopenalex-snapshot
References
inferred← citeshttps://doi.org/10.1002/9780471264194.fos06135openalex-snapshot
Lead tetraacetate ( LTA )
inferred← citeshttps://doi.org/10.1002/9781118662083.cot05-011openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/advs.74920openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/asia.202000092openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chin.197609096openalex-snapshot
ChemInform Abstract: REACTIONS OF AMINES. XVIII. OXIDATIVE REARRANGEMENT OF AMIDES WITH LEAD TETRAACETATE
inferred← citeshttps://doi.org/10.1002/cjoc.201090071openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cssc.202400234openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/hc.5openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/hlca.19940770419openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/jctb.280590310openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/jlac.198419840906openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/tcr.20084openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/7081_2007_063openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-1-4613-2109-5_14openalex-snapshot
Oxidations with Lead Tetraacetate
inferred← citeshttps://doi.org/10.1007/978-3-322-94015-5_56openalex-snapshot
Hofmann-Umlagerung
inferred← citeshttps://doi.org/10.1007/978-3-322-94077-3_57openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-322-94726-0_56openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-322-96805-0_9openalex-snapshot
H
inferred← citeshttps://doi.org/10.1007/bf02974108openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf03036864openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0008-6215(91)80151-copenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0040-4039(90)80016-fopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0091-3057(87)90176-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b0-08-044655-8/00116-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b0-08-044705-8/00247-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b0-08-044705-8/09013-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-08-052349-1.00172-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-697253-5.50006-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-823743-4.33003-9openalex-snapshot
The Hofmann rearrangement
inferred← citeshttps://doi.org/10.1016/j.bmcl.2007.10.010openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jfluchem.2015.05.007openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.mcat.2024.113823openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.molstruc.2006.11.038openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2003.10.109openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2010.09.073openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetasy.2010.03.022openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2005.05.077openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.11.134openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.01.126openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.04.011openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.01.025openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2021.153422openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2023.154494openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2023.154683openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0008-6215(92)84239-oopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0013-4686(00)00380-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0014-827x(02)01234-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0022-1139(00)80183-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4020(01)91030-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4020(02)01053-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4020(97)00791-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4020(97)00920-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4039(00)61770-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4039(00)79971-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4039(00)82424-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4039(00)85230-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4039(00)95460-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4039(01)00895-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4039(01)00985-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4039(02)01853-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4039(96)02341-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4039(97)00324-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4039(97)10324-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4039(98)00342-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0378-5173(98)00241-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0957-4166(96)00457-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.iecr.9b02438openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jmedchem.9b01541openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ja972744ropenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ja991683popenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jm300349jopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jm501371sopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jm981126yopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jo010456eopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jo048408sopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jo0619074openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jo101504eopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jo9708553openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jo981816+openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ma981618kopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ol0608799openalex-snapshot
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inferred← citeshttps://doi.org/10.1039/a703387gopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/a904126eopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/a907337jopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/b801909fopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/p19940002975openalex-snapshot
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inferred← citeshttps://doi.org/10.1080/00397918908052588openalex-snapshot
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inferred← citeshttps://doi.org/10.1080/00397919608003656openalex-snapshot
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inferred← citeshttps://doi.org/10.1080/07328318708056201openalex-snapshot
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inferred← citeshttps://doi.org/10.1246/cl.1982.565openalex-snapshot
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inferred← citeshttps://doi.org/10.1246/cl.1989.463openalex-snapshot
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inferred← citeshttps://doi.org/10.1515/ncrs-2000-0168openalex-snapshot
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inferred← citeshttps://doi.org/10.1515/ncrs-2016-0077openalex-snapshot
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inferred← citeshttps://doi.org/10.2174/1385272823666191023115842openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fmolb.2022.983679openalex-snapshot
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