Synthesis and reactivity of heterocyclic hydroxylamine-O-sulfonates
Cu(OTf)2-Catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA)
![PDF] Cu(OTf)2-Catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA) | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/0615b0928d07b0fb565394b813ca3929843b6cea/2-Table1-1.png "PDF] Cu(OTf)2-Catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA) | Semantic Scholar")
PDF] Cu(OTf)2-Catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA) | Semantic Scholar
Dichloroimidazolidinedione-Activated Beckmann Rearrangement of Ketoximes for Accessing Amides and Lactams | The Journal of Organic Chemistry
Cu(OTf)2-catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA).,Synthesis - X-MOL
![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](https://pubs.rsc.org/image/article/2002/P1/b108164k/b108164k-s3.gif "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")
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
![PDF] Cu(OTf)2-Catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA) | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/0615b0928d07b0fb565394b813ca3929843b6cea/1-Figure1-1.png "PDF] Cu(OTf)2-Catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA) | Semantic Scholar")
PDF] Cu(OTf)2-Catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA) | Semantic Scholar
Dichloroimidazolidinedione-Activated Beckmann Rearrangement of Ketoximes for Accessing Amides and Lactams | The Journal of Organic Chemistry
Beckmann Rearrangement – Master Organic Chemistry
Direct synthesis of secondary amides from ketones through Beckmann rearrangement using O-(mesitylsulfonyl)hydroxylamine - ScienceDirect
Beckmann rearrangement catalysis: a review of recent advances - New Journal of Chemistry (RSC Publishing) DOI:10.1039/D0NJ02034F
Hydroxylamine-mediated C–C amination via an aza-hock rearrangement | Nature Communications
Hydroxylamine-O-sulfonic acid - Wikipedia
Beckmann Reaction - an overview | ScienceDirect Topics
Beckmann Rearrangement
Hydroxylamine-O-sulfonic acid - Wikipedia
Beckmann Rearrangement
Beckmann rearrangement - Wikipedia
Hydroxylamine-mediated C–C amination via an aza-hock rearrangement | Nature Communications
The Mechanochemical Beckmann Rearrangement: An Eco-efficient “Cut-and-Paste” Strategy to Design the “Good Old Amide Bond” | ACS Sustainable Chemistry & Engineering
Mechanistic Insight into Self-Propagation of Organo-Mediated Beckmann Rearrangement: A Combined Experimental and Computational Study | The Journal of Organic Chemistry
Zinc(II)-Catalyzed Synthesis of Secondary Amides from Ketones via Beckmann Rearrangement Using Hydroxylamine-O-sulfonic Acid in Aqueous Media
Hydroxylamine-O-sulfonic acid - Wikipedia
Cu(II)-Catalyzed Beckmann Rearrangement of Ketones
Beckmann Rearrangement of Ketoximes to Lactams by Triphosphazene Catalyst | The Journal of Organic Chemistry
The Mechanochemical Beckmann Rearrangement: An Eco-efficient “Cut-and-Paste” Strategy to Design the “Good Old Amide Bond” | ACS Sustainable Chemistry & Engineering
