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2012
DOI: 10.1080/00397911.2011.573172
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Ceric Ammonium Nitrate as the Novel Oxidizing Agent for the Facile Synthesis of (Dichloroiodo)arenes

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Cited by 6 publications
(3 citation statements)
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“…According to Tale et al . , the reaction of CAN with HCl generates in situ molecular chlorine, causing oxidative conversion of iodoarenes to (dichloroiodo) arenes. Similarly, Hwu and King concluded that CAN is responsible for enhanced destruction of other functional groups in the presence of acids like hydrogen chloride, hydrogen bromide, acetic acid, etc.…”
Section: Resultsmentioning
confidence: 97%
“…According to Tale et al . , the reaction of CAN with HCl generates in situ molecular chlorine, causing oxidative conversion of iodoarenes to (dichloroiodo) arenes. Similarly, Hwu and King concluded that CAN is responsible for enhanced destruction of other functional groups in the presence of acids like hydrogen chloride, hydrogen bromide, acetic acid, etc.…”
Section: Resultsmentioning
confidence: 97%
“…[309][310][311] For instance, the reaction of 1 with CAN and cyclodienes in acetonitrile resulted in the formation of 1,4-and 1,2-furonaphthoquinones (151)(152)(153)(154), as presented in Scheme 41. CAN, a well know one-electron oxidant, 307,308 easily handled and soluble in various solvents, is very useful in many reactions.…”
Section: Synthesis Of Other Heterocycles From Lawsone (1)mentioning
confidence: 99%
“…CAN, a well know one-electron oxidant, 307,308 easily handled and soluble in various solvents, is very useful in many reactions. [309][310][311] For instance, the reaction of 1 with CAN and cyclodienes in acetonitrile resulted in the formation of 1,4-and 1,2-furonaphthoquinones (151)(152)(153)(154), as presented in Scheme 41. 312 Additionally, manganese(III) acetate dihydrate can promote the radical cyclization of 1 with alkenes, leading selectively to 1,4-furonaphthoquinones (155a-d) in excellent yields (Scheme 41).…”
Section: Synthesis Of Other Heterocycles From Lawsone (1)mentioning
confidence: 99%