2010
DOI: 10.1080/00397910903219310
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Accelerated Amination of Baylis–Hillman Acetates Under Ultrasound Irradiation

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Cited by 4 publications
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“…From another perspective, the Morita–Baylis–Hillman (MBH) reaction has emerged in recent decades as one of the most sought after reactions for the synthesis of various multifunctional scaffolds . The MBH acetates of electron-deficient alkenes have been subjected to substitution, often S N 2′, by numerous nucleophiles including amines under uncatalyzed, organocatalyzed and metal-catalyzed conditions. However, to our knowledge, synthesis of imidazopyridines from the MBH adducts of electron-deficient alkenes, including nitroalkenes, remains unreported …”
mentioning
confidence: 99%
“…From another perspective, the Morita–Baylis–Hillman (MBH) reaction has emerged in recent decades as one of the most sought after reactions for the synthesis of various multifunctional scaffolds . The MBH acetates of electron-deficient alkenes have been subjected to substitution, often S N 2′, by numerous nucleophiles including amines under uncatalyzed, organocatalyzed and metal-catalyzed conditions. However, to our knowledge, synthesis of imidazopyridines from the MBH adducts of electron-deficient alkenes, including nitroalkenes, remains unreported …”
mentioning
confidence: 99%