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A new odorless one-pot synthesis of thioesters and selenoesters promoted by Rongalite®

https://doi.org/10.1016/j.tet.2010.07.023
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/1521-3773(20001002)39:19<3348::aid-anie3348>3.0.co;2-xopenalex-snapshot
Artificial Molecular Machines
inferredcites →https://doi.org/10.1002/adsc.200505122openalex-snapshot
Ionic Liquid as Catalyst and Reaction Medium: A Simple, Convenient and Green Procedure for the Synthesis of Thioethers, Thioesters and Dithianes using an Inexpensive Ionic Liquid, [pmIm]Br
inferredcites →https://doi.org/10.1002/anie.200501606openalex-snapshot
Tin‐Free Radical Carbonylation: Thiol Ester Synthesis Using Alkyl Allyl Sulfone Precursors, Phenyl Benzenethiosulfonate, and CO
inferredcites →https://doi.org/10.1007/s00706-002-0545-0openalex-snapshot
Synthesis of Selenol Esters from Acid Chlorides and Organic Diselenides in the Presence of the Zn/AlCl 3 System
inferredcites →https://doi.org/10.1007/s007060200078openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.jorganchem.2010.01.025openalex-snapshot
Air-stable titanocene bis(perfluorooctanesulfonate) as a new catalyst for acylation of alcohols, phenols, thiols, and amines under solvent-free condition
inferredcites →https://doi.org/10.1016/j.molcata.2006.04.026openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.molcata.2008.04.010openalex-snapshot
Solid trichlorotitanium(IV) trifluoromethanesulfonate TiCl3(OTf) catalyzed efficient acylation of –OH and –SH: Direct esterification of alcohols with carboxylic acids and transesterification of alcohols with esters under neat conditions
inferredcites →https://doi.org/10.1016/j.tet.2009.01.072openalex-snapshot
Indium-mediated cleavage of diphenyl diselenide and diphenyl disulfide: efficient one-pot synthesis of unsymmetrical diorganyl selenides, sulfides, and selenoesters
inferredcites →https://doi.org/10.1016/j.tet.2009.03.069openalex-snapshot
Efficient synthesis of selenol esters from acid chlorides mediated by indium metal
inferredcites →https://doi.org/10.1016/j.tet.2009.04.085openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.tet.2010.02.001openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.tetlet.2006.12.024openalex-snapshot
Dess–Martin periodinane mediated synthesis of thioesters from aldehydes
inferredcites →https://doi.org/10.1016/j.tetlet.2008.01.109openalex-snapshot
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Studies in heterocyclic chemistry—I
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trans-1,3-dithiane-1,3-dioxide; a chiral acyl anion equivalent. Enantioselective synthesis of α-hydroxy- carboxylic acids, esters, amides and ketones
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inferredcites →https://doi.org/10.1055/s-1985-31259openalex-snapshot
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What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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inferred← citeshttps://doi.org/10.1002/9780470682531.pat0716openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/adsc.201200227openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ajoc.202000077openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.201400185openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.202005430openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.202203716openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chin.201052087openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cjoc.201200028openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cplu.202400183openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ejoc.201300295openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ejoc.202200452openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ejoc.202401399openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/jhet.1043openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00706-020-02565-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12039-012-0305-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12039-020-01871-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.11363-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-443-31482-7.00007-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.scp.2026.102464openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2013.01.024openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2019.130624openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2024.133978openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.09.132openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.04.041openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.joc.0c02328openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jpca.3c01624openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s44160-023-00353-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c1gc16243hopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c2gc16541dopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c4ra07983copenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d3ob01991hopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d4ra08769kopenalex-snapshot
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inferred← citeshttps://doi.org/10.1080/17415993.2015.1075023openalex-snapshot
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inferred← citeshttps://doi.org/10.1139/v09-043openalex-snapshot
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inferred← citeshttps://doi.org/10.1515/psr-2017-0129openalex-snapshot
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