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ChemInform Abstract: Multicomponent Reaction of Z‐Chlorooximes, Isocyanides, and Hydroxylamines as Hypernucleophilic Traps. A One‐Pot Route to Aminodioximes and Their Transformation into 5‐Amino‐1, 2, 4‐oxadiazoles by Mitsunobu—Beckmann Rearrangement. Issue 9 (February 2016)
Record Type:
Journal Article
Title:
ChemInform Abstract: Multicomponent Reaction of Z‐Chlorooximes, Isocyanides, and Hydroxylamines as Hypernucleophilic Traps. A One‐Pot Route to Aminodioximes and Their Transformation into 5‐Amino‐1, 2, 4‐oxadiazoles by Mitsunobu—Beckmann Rearrangement. Issue 9 (February 2016)
Main Title:
ChemInform Abstract: Multicomponent Reaction of Z‐Chlorooximes, Isocyanides, and Hydroxylamines as Hypernucleophilic Traps. A One‐Pot Route to Aminodioximes and Their Transformation into 5‐Amino‐1, 2, 4‐oxadiazoles by Mitsunobu—Beckmann Rearrangement.
Abstract: A three‐component coupling reaction of Z‐chloro oximes, isocyanides, and hydroxylamine affords aminoglyoximes via [3+1] cycloaddition with preferential attack of isocyanides to nitrile N‐oxides.