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- Wikipedia
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Cu(OTf)<sub>2</sub>-catalyzed Beckmann Rearrangement of Ketones Hydroxylamine<i>-O-</i>sulfonic Acid - Abstract - Europe PMC
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Synthesis and heterocyclic hydroxylamine-O-sulfonates
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Synthesis Secondary Amides from Ketones via Beckmann Rearrangement Using Hydroxylamine-O-sulfonic Acid in Aqueous - X-MOL
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- Wikiwand
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- Wikiwand
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Hydroxylamine-mediated C–C amination aza-hock | Nature Communications
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Cu(OTf)2-catalyzed Beckmann Rearrangement of Using Hydroxylamine-O-sulfonic Acid (HOSA). Semantic Scholar
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- Wikiwand
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Hydroxylamine-O-sulfonic acid | H3NO4S PubChem
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acid (CAS 2950-43-8) Glentham Life Sciences
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- Wikipedia
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- Wikiwand
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Cu(OTf)<sub>2</sub>-catalyzed Beckmann Rearrangement of Ketones Hydroxylamine<i>-O-</i>sulfonic Acid - Abstract - Europe PMC
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Cu(OTf)<sub>2</sub>-catalyzed Beckmann Rearrangement of Ketones Hydroxylamine<i>-O-</i>sulfonic Acid - Abstract - Europe PMC
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Rearrangement
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- Wikipedia
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Synthesis of 6-alkyl of the 1-azabicyclo[4.3.0]nonan-2-one system by a strategy of geminal acylation Beckmann rearrangement - Journal of the Chemical Society, Perkin Transactions 1 (RSC Publishing)
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Synthesis and heterocyclic hydroxylamine-O-sulfonates
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Cu(OTf)2-catalyzed Beckmann Rearrangement of Using Hydroxylamine-O-sulfonic Acid (HOSA). Semantic Scholar
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oxime formation-Beckmann | Download Table