An efficient deprotection of dithioacetals to carbonyls using Oxone-KBr in aqueous acetonitrile

A simple and efficient method has been developed for the chemoselective dethioacetalization of dithioacetals to aldehydes and ketones using Oxone-KBr in aqueous acetonitrile at room temperature.     

2,6‐Dicarboxypyridinium Fluorochromate: A Mild and Efficient Reagent for Oxidative Deprotection of Oximes,Phenylhydrazones, and Semicarbazones to Their Corresponding Carbonyl Compounds under Solvent‐Free Conditions

2,6‐Dicarboxypyridinium fluorochromate as a new, rapid, and efficient reagent was prepared and used for the oxidative deprotection of oximes, phenylhydrazones, and semicarbazones to their carbonyl analogues under solvent‐free conditions at room temperature.     

Mild and efficient tetrahydropyranylation of alcohols and dehydropyranylation of THP ethers catalyzed by ferric perchlorate

A simple, mild and efficient method for tetrahydropyranylation and dehydropyranylation of alcohols in the presence of ferric perchlorate are described.     

Synthesis and characterization ofα-butyl-ω-{3-[(2,2-dihydroxymethyl)-propionyloxy]}propylpolydimethylsiloxanes

A series of polydimethylsiloxanes containing two primary hydroxyl groups at one single chain end were synthesized by five-step reactions which included esterification, hydroxyl protection, anionic ring-opening polymerization, hydrosilylation and deprotection. The prepared compounds in each step were characterized. The results showed that each step synthesis was successfully carried out and objective products could be achieved.     

An Efficient and Mild Deprotection of 1,3-Oxathiolanes to Carbonyl Compounds Using the Superoxide Ion

An efficient deprotection of 1,3-oxathiolanes to carbonyl compounds has been achieved under the mild reaction conditions of tetraethylammonium superoxide in an aprotic medium at room temperature.     

DIRECT OXIDATIVE DEPROTECTION USING MONTMORILLONITE SUPPORTED AMMONIUM CHLOROCHROMATE UNDER CONVENTIONAL HEATING AND MICROWAVE IRRADIATION IN SOLVENTLESS SYSTEM

Abstract

Trimethylsilyl ethers are selectively and rapidly oxidized to the corresponding carbonyl compounds by montmorillonite k-10 supported ammonium chlorochromate under conventional heating and microwave irradition in solvent free condition.     

The Economic Synthesis of Pyridinium Fluorochromate(VI), C5H5NH[CrO3F] (PFC), and Solvent‐Free Oxidation of Organic Substrates with PFC

Abstract

A 1:1:1 stoichiometric reaction among CrO₃, aqueous HF and pyridine affords orange crystalline pyridinium fluorochromate(VI), C₅H₅NH[CrO₃F] (PFC), in 99.2% isolated yield. The reagent under solvent‐free conditions readily converts benzylic, secondary, and allylic alcohols to the corresponding carbonyls and selectively oxidizes secondary alcohols in the presence of primary alcohols, polycyclic hydrocarbons to cyclic ketones, benzoin to benzil, PPh₃ to O?PPh₃, methylphenyl sulfide to sulfoxide, cyclohexanone oxime to cyclohexanone, an allylic Δ⁵‐steroid to the corresponding α,β‐unsaturated ketone and deprotects dioxolanes and dithiolanes to aldehydes; the economic synthesis of PFC, its ease of reaction without solvent, versatility, and high isolated yields of the products are the significant features of the protocol.     

Facile deprotection of dithioacetals by using a novel 1,4-benzoquinone/cat. NaI system

The combination of 1,4-benzoquinone and a catalytic amount of NaI was found to be effective for the deprotection of dithioacetals. The reactions proceeded efficiently under mild, near-neutral reaction conditions, producing a wide range of aryl and alkyl aldehydes and ketones generally in high yields with good functional group compatibility. The method developed therefore represents a general, facile, and highly applicable approach for deprotecting dithioacetals.     

N‐Benzyl‐DABCO‐tribromide as an efficient and mild reagent for deprotection of dithioacetals

N‐Benzyl‐DABCO‐ammonium tribromide was found to be an efficient and recyclable reagent for the deprotection of dithioacetals in dichloromethane/methanol at room temperature. The reaction can be performed cleanly, in short time, and in high yield.