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Iron (III) Phosphate as a Green and Reusable Catalyst Promoted Chemo Selective Acetylation of Alcohols and Phenols with Acetic Anhydride Under Solvent Free Conditions at Room Temperature

https://doi.org/10.5012/jkcs.2011.55.4.633
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/978-1-4684-7218-9openalex-snapshot
Protective Groups in Organic Chemistry
inferredcites →https://doi.org/10.1016/b978-0-08-018786-0.50001-4openalex-snapshot
Comprehensive Inorganic Chemistry
inferredcites →https://doi.org/10.1016/j.catcom.2005.09.011openalex-snapshot
Catalytic acetylation of alcohols and phenols with ferric perchlorate in acetic acid
inferredcites →https://doi.org/10.1016/j.molcata.2006.02.057openalex-snapshot
H14[NaP5W30O110]: A heteropoly acid catalyzed acetylation of alcohols and phenols in acetic anhydride
inferredcites →https://doi.org/10.1016/s0040-4020(01)01229-7openalex-snapshot
Lewis acid catalyzed acylation reactions: scope and limitations
inferredcites →https://doi.org/10.1016/s0926-860x(01)00837-7openalex-snapshot
Direct conversion of methane into oxygenates
inferredcites →https://doi.org/10.1021/jo00033a020openalex-snapshot
Cobalt(II) chloride catalyzed acylation of alcohols with acetic anhydride: scope and mechanism
inferredcites →https://doi.org/10.1021/jo0107453openalex-snapshot
Highly Powerful and Practical Acylation of Alcohols with Acid Anhydride Catalyzed by Bi(OTf)3
inferredcites →https://doi.org/10.1021/jo952237xopenalex-snapshot
Scandium Trifluoromethanesulfonate as an Extremely Active Lewis Acid Catalyst in Acylation of Alcohols with Acid Anhydrides and Mixed Anhydrides
inferredcites →https://doi.org/10.1021/jo980011zopenalex-snapshot
An Extremely Powerful Acylation Reaction of Alcohols with Acid Anhydrides Catalyzed by Trimethylsilyl Trifluoromethanesulfonate
inferredcites →https://doi.org/10.1080/00397919708005028openalex-snapshot
Chlorotrimethylsilane Catalysed Acylation of Alcohols1
inferredcites →https://doi.org/10.1246/bcsj.66.1516openalex-snapshot
A New and Efficient Esterification Reaction via Mixed Anhydrides by the Promotion of a Catalytic Amount of Lewis Acid
inferredcites →https://doi.org/10.1515/hc.2006.12.5.369openalex-snapshot
IRON (III) PHOSPHATE DIHYDRATE - CATALYZED ONE-POT SYNTHESIS OF DIHYDROPYRIMIDINONES AND THIONES : AN IMPROVED PROCEDURE FOR THE BIGINELLI REACTION
inferredcites →https://doi.org/10.1590/s0103-50532006000500033openalex-snapshot
Copper(II) sulfate pentahydrate (CuSO4.5H2O): a green catalyst for solventless acetylation of alcohols and phenols with acetic anhydride
inferredcites →https://doi.org/10.3987/com-10-12019openalex-snapshot
Anhydrous FePO4: A Green and Cost-Effective Catalyst for the One-Pot Three Component Synthesis of 2,4,5-Triarylated Imidazoles

What points at this work

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inferred← citeshttps://doi.org/10.2139/ssrn.3983581openalex-extracted
A new catalyst for the synthesis of 2-substituted perimidines catalyzed by FePO4[enter Paper Title]
inferred← citeshttps://doi.org/10.1007/s10593-012-1093-0openalex-snapshot
One-pot synthesis of 2-substituted benzimidazoles catalyzed by anhydrous FePO4
inferred← citeshttps://doi.org/10.1007/s10934-015-0077-8openalex-snapshot
Synthesis of tert-butyl acetate via eco-friendly additive reaction over mesoprous silica catalysts with balanced Brönsted and Lewis acid sites
inferred← citeshttps://doi.org/10.1016/j.jtusci.2015.10.004openalex-snapshot
A new catalyst for the synthesis of 2-substituted perimidines catalysed by FePO4
inferred← citeshttps://doi.org/10.1021/acs.jced.7b01021openalex-snapshot
Isobaric Vapor–Liquid Equilibrium for Binary and Ternary Systems of tert-Butanol + tert-Butyl Acetate + Chlorobenzene at 101.33 kPa
inferred← citeshttps://doi.org/10.1021/jo501886wopenalex-snapshot
Decarboxylative-Coupling of Allyl Acetate Catalyzed by Group 10 Organometallics, [(phen)M(CH3)]+
inferred← citeshttps://doi.org/10.1080/10426507.2013.844142openalex-snapshot
Rice Husk Ash: A New, Cheap, Efficient, and Reusable Reagent for the Protection of Alcohols, Phenols, Amines, and Thiols
inferred← citeshttps://doi.org/10.1134/s1070427214100176openalex-snapshot
Solvent-free synthesis of 4,4′-diaminotriarylmethanes-leuco malachite materials in the presence of FePO4
inferred← citeshttps://doi.org/10.47116/apjcri.2022.10.16openalex-snapshot
Kinetics and Mechanism of the Oxidation of Substituted Benzyl Alcohols by (C9H7NH)2Cr2O7
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