Hydroxylamine-mediated C–C amination via an aza-hock rearrangement | Nature Communications
Hydroxylamine-mediated C–C amination via an aza-hock rearrangement | Nature Communications
Beckmann Rearrangement
The Mechanochemical Beckmann Rearrangement: An Eco-efficient “Cut-and-Paste” Strategy to Design the “Good Old Amide Bond” | ACS Sustainable Chemistry & Engineering
Beckmann Rearrangement
Hydroxylamine-O-sulfonic acid - Wikipedia
Beckmann Rearrangement of Ketoximes to Lactams by Triphosphazene Catalyst | The Journal of Organic Chemistry
Mechanistic Insight into Self-Propagation of Organo-Mediated Beckmann Rearrangement: A Combined Experimental and Computational Study | The Journal of Organic Chemistry
Cu(OTf)2-catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA). - Abstract - Europe PMC
Hydroxylamine-mediated C–C amination via an aza-hock rearrangement | Nature Communications
Hydroxylamine-mediated C–C amination via an aza-hock rearrangement | Nature Communications
Cu(OTf)2-Catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA)
Beckmann rearrangement catalysis: a review of recent advances - New Journal of Chemistry (RSC Publishing) DOI:10.1039/D0NJ02034F
PDF] Cu(OTf)2-Catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA) | Semantic Scholar
Synthesis and reactivity of heterocyclic hydroxylamine-O-sulfonates
Hydroxylamine-O-sulfonic acid - Wikipedia
Dichloroimidazolidinedione-Activated Beckmann Rearrangement of Ketoximes for Accessing Amides and Lactams | The Journal of Organic Chemistry
Direct synthesis of secondary amides from ketones through Beckmann rearrangement using O-(mesitylsulfonyl)hydroxylamine - ScienceDirect
Synthesis of 6-alkyl analogues of the 1-azabicyclo[4.3.0]nonan-2-one system by a strategy of geminal acylation and Beckmann rearrangement - Journal of the Chemical Society, Perkin Transactions 1 (RSC Publishing) DOI:10.1039/B108164K
Hydroxylamine-O-sulfonic acid - Wikipedia
Direct synthesis of secondary amides from ketones through Beckmann rearrangement using O-(mesitylsulfonyl)hydroxylamine - ScienceDirect
Zinc(II)-Catalyzed Synthesis of Secondary Amides from Ketones via Beckmann Rearrangement Using Hydroxylamine-O-sulfonic Acid in Aqueous Media
Scope and Mechanism of a True Organocatalytic Beckmann Rearrangement with a Boronic Acid/Perfluoropinacol System under Ambient Conditions | Journal of the American Chemical Society
Cu(OTf)2-Catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA)