Hydroxylamine-O-sulfonic acid - Wikipedia
Scope and Mechanism of a True Organocatalytic Beckmann Rearrangement with a Boronic Acid/Perfluoropinacol System under Ambient Conditions | Journal of the American Chemical Society
Beckmann Rearrangement – Master Organic Chemistry
Hydroxylamine-O-sulfonic acid - Wikipedia
Hydroxylamine-mediated C–C amination via an aza-hock rearrangement | Nature Communications
Beckmann Rearrangement – Master Organic Chemistry
Cu(OTf)2-Catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA)
Cu(OTf)2-Catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA)
Cu(OTf)2-catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA). - Abstract - Europe PMC
The Mechanochemical Beckmann Rearrangement: An Eco-efficient “Cut-and-Paste” Strategy to Design the “Good Old Amide Bond” | ACS Sustainable Chemistry & Engineering
Hydroxylamine-O-sulfonic acid - Wikipedia
Hydroxylamine-O-sulfonic acid - Wikipedia
Beckmann rearrangement - Wikipedia
Synthesis and reactivity of heterocyclic hydroxylamine-O-sulfonates
Beckmann Reaction - an overview | ScienceDirect Topics
Cu(OTf)2-catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA).,Synthesis - X-MOL
Table 3 from Mild, calcium catalysed Beckmann rearrangements. | Semantic Scholar
Zinc(II)-Catalyzed Synthesis of Secondary Amides from Ketones via Beckmann Rearrangement Using Hydroxylamine-O-sulfonic Acid in Aqueous Media,Synthesis - X-MOL
Cu(II)-Catalyzed Beckmann Rearrangement of Ketones
Beckmann Rearrangement
Beckmann Rearrangement – Master Organic Chemistry
Beckmann Rearrangement Reaction - Online Organic Chemistry Tutor
Hydroxylamine-mediated C–C amination via an aza-hock rearrangement | Nature Communications
Zinc(II)-Catalyzed Synthesis of Secondary Amides from Ketones via Beckmann Rearrangement Using Hydroxylamine-O-sulfonic Acid in Aqueous Media
Synthesis and reactivity of heterocyclic hydroxylamine-O-sulfonates
Beckmann Rearrangement – Master Organic Chemistry
