Organic Syntheses Procedure
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Alcohols are converted to tosylates by treatment with p-toluence sulfonyl chloride (TsCl) in the presence of pyridine. This overall process converts a poor leaving group (overset(Ө)H) into good one (overset(Ө)Ts). A tosylate
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N-Sulfonylation of amines, imides, amides and anilides using p-TsCl in presence of atomized sodium in EtOH–THF under sonic condition - ScienceDirect
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Tosyl group - Wikipedia
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Organic Syntheses Procedure
p-Toluenesulfonyl chloride ReagentPlus�, = 99 98-59-9
Alcohols are converted to tosylates by treatment with p-toluence sulfonyl chloride (TsCl) in the - YouTube
What is Tosyl chloride?_Chemicalbook
4-Toluenesulfonyl chloride - Wikipedia
Reagent Friday: TsCl (p-toluenesulfonyl chloride) and MsCl (methanesulfonyl chloride) – Master Organic Chemistry
P-Toluenesulfonyl chloride | C7H7ClO2S - PubChem
Tosyl chloride | C7H7ClO2S | ChemSpider
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98-59-9 | p-Toluenesulfonyl Chloride | p-Toluenesulfonyl Chloride; 4-Methylbenzene-1-sulfonyl Chloride; 4-Methylbenzenesulfonyl Chloride; 4-Methylphenylsulfonyl Chloride; 4-Toluenesulfonyl Chloride; 4-Toluolsulfonyl Chloride; 4-Tosyl Chloride; NSC ...
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Reagent Friday: TsCl (p-toluenesulfonyl chloride) and MsCl (methanesulfonyl chloride) – Master Organic Chemistry
