Revisiting the Solution Structure of Ceric Ammonium Nitrate

Ceric ammonium nitrate (CAN) is a single‐electron‐transfer reagent with unparalleled utility in organic synthesis, and has emerged as a vital feedstock in diverse chemical industries. Most applications use CAN in solution where it is assigned a monomeric [Ce^IV(NO₃)₆]^2? structure; an assumption traced to half‐century old studies. Using synchrotron X‐rays and Raman spectroscopy we challenge this tradition, converging instead on an oxo‐bridged dinuclear complex, even in strong nitric acid. Thus, one equivalent of CAN is recast as a two‐electron‐transfer reagent and a redox‐activated superbase, raising questions regarding the origins of its reactivity with organic molecules and giving new fundamental insight into the stability of polynuclear complexes of tetravalent ions.     

Ceric Ammonium Nitrate Catalyzed Oxidation of Aldehydes and Alcohols

A variety of aromatic, aliphatic and conjugated aldehydes and alcohols were transformed to the corresponding carboxylic acids and ketones with a quantitative conversion in high yields with 70% t‐BuOOH solution in water in the presence of catalytic amounts of ceric ammonium nitrate [Ce(NH₄)₂(NO₃)₆] (CAN) under room temperature conditions. The scope of our catalytic system is applicable for a wide range of aromatic, conjugated and aliphatic substrates. These aldehydes were converted to the corresponding carboxylic acids in good isolated yields in reasonable times. This method possesses a wide range of capabilities since it can be used with other functional groups which may not tolerate oxidative conditions, involves fairly simple method for work‐up, exhibits chemoselectivity and proceeds under ambient conditions. The resulting products are obtained in good yields within reasonable time.     

Facile Route to Tetrasubstituted Pyrazoles Utilizing Ceric Ammonium Nitrate

A convenient approach for the synthesis of tetrasubstituted pyrazoles is described. The method involves the treatment of 1,3-diketones and allyltrimethylsilane with CAN followed by cerium-catalyzed addition of substituted hydrazines to construct pyrazoles in good yields.     

硝酸铈铵中铈的价态分析

讨论了硝酸铈铵中铈的价态分析问题.硫酸亚铁铵法测定样品中的四价铈含量;盐酸羟胺还原四价铈后,EDTA法滴定样品中总铈含量;总铈含量与四价铈含量之差为样品中三价铈含量.     

Ceric Ammonium Nitrate in Organic Synthesis III. A Facile Synthesis of Methoxylated 3, 4 Dihydroisoquinolinium Nitrates

A mild and efficient method for the synthesis of 3, 4-dihydroisoquinolinium salts, key intermediates for the preparation of isoquinoline alkaloïds, by an oxidation of N-methyl-1, 2, 3, 4-tetrahydroisoquinolines using ceric ammonium nitrate (CAN) is described.     

Highly Regio- and Stereoselective Synthesis of β-Halohydrins from Epoxides Catalyzed with Ceric Ammonium Nitrate

Ce(IV) as ceric ammonium nitrate can effectively catalyze ring opening of epoxides with halides under very mild conditions and easy procedure to give the corresponding β-chloro-and β-bromohydrins in excellent yields. The reactions occur with both substituted and unsubstituted quaternary ammonium halides and with high regio- and stereoselectivity. The reaction of optically active styrene oxide with chloride ion was found to be highly stereospecific and afforded the corresponding β-halohydrin in 96% ee.     

Ceric Ammonium Nitrate as the Novel Oxidizing Agent for the Facile Synthesis of (Dichloroiodo)arenes

Ceric ammonium nitrate (CAN) has been found to be a remarkable oxidizing agent for the oxidative conversion of iodoarenes to (dichloroiodo)arenes in acetic acid using aqueous HCl. The reaction of CAN with HCl generates in situ molecular chlorine, which is responsible for the oxidation. This method avoids the use of hazardous, toxic, and corrosive gaseous chlorine.     

季铵型硝化纤维素的合成及应用

高分子吸附剂;肌酸酐;季铵型硝化纤维素的合成及应用     

Tandem Oxidation Process Using Ceric Ammonium Nitrate: Three-Component Synthesis of Trisubstituted Imidazoles Under Aerobic Oxidation Conditions

By combining a ceric ammonium nitrate (CAN)–catalyzed aerobic oxidation of α-hydroxy ketones with a subsequent three-component condensation reaction using aldehydes and ammonium acetate, highly substituted imidazole derivatives can be assembled. This reaction is an important approach for the synthesis of highly substituted imidazole derivatives and was carried out in good to excellent yields in ethanol as an environmentally benign solvent.     

Ceric Ammonium Nitrate (CAN)–Catalyzed Multicomponent Reactions: An Efficient Catalyst for Green Organic Synthesis

Multicomponent reactions (MCRs) consist of two or more synthetic steps carried out without isolation of any intermediate, which reduces time and saves money, energy, and raw materials. The development of MCRs in the presence of ceric ammonium nitrate (CAN) is an efficient approach that meets with requirements of sustainable chemistry. The aim of this review is to highlight the interactive effect of the combined use of MCRs and CAN for the development of new ecofavorable methodologies for synthetic organic chemistry. There are many advantages to the use of CAN as a catalyst in organic synthesis, including the very small amount of this catalyst needed to complete reactions in most cases, lower costs, ecofriendly nature, ease of handling, nontoxicity, and high reactivity.     

Synthesis of 3-Acyl and 3-Carboalkoxyfurans by the Ceric Ammonium Nitrate Promoted Addition of 1,3-Dicarbonyl Compounds to Vinylic Acetates

3-Acyl- and 3-carboalkoxyfurans can be prepared in 30–55% yield by the oxidative addition of 1,3-dicarbonyl compounds to vinylic acetates induced by eerie ammonium nitrate.     

Ceric Ammonium Nitrate (CAN) catalyzes the one-pot synthesis of polyhydroquinoline via the Hantzsch reaction

A facile and efficient one-pot synthesis of high yields of polyhydroquinoline derivatives at ambient temperature using Ceric Ammonium Nitrate (CAN) as catalyst via the Hantzsch reaction was reported. The process is simple and environmentally benign and the catalyst is commercially available and inexpensive.     

Ceric Ammonium Nitrate Catalysed Protection of Alcohols by 3, 4-Dihydro-2H-pyran

Hydroxyl compounds readily add to dihydropyran in presence of a catalytic amount of ceric ammonium nitrate to give high yield of tetrahydropyranyl ethers.     

Oxidative Cyclization of Unsaturated Ketene Dithioacetals with Ceric Ammonium Nitrate to Form Bicyclic Lactones

Ceric ammonium nitrate oxidizes unsaturated ketene dithioacetals in wet MeCN to give cation radicals that cyclize to trisubstituted double bonds and styrenes by cation-like cyclizations leading to cyclic cation radicals that are transformed by further oxidation, hydrolysis and cyclization to bicyclic lactones in moderate to good yield.