Synthesis and reactivity of heterocyclic hydroxylamine-O-sulfonates in: Heterocyclic Communications Volume 20 Issue 3 (2014)
Hydroxylamine-O-sulfonic acid - Wikiwand
Cu(II)-Catalyzed Beckmann Rearrangement of Ketones
The photochemical Beckmann rearrangement
Synthesis of a tricyclic lactam via Beckmann rearrangement and ring-rearrangement metathesis as key steps. - Abstract - Europe PMC
Dichloroimidazolidinedione-Activated Beckmann Rearrangement of Ketoximes for Accessing Amides and Lactams - J. Org. Chem. - X-MOL
Hydroxylamine-O-sulfonic acid - Wikiwand
Hydroxylamine-O-sulfonic acid - Wikiwand
Hydroxylamine-O-sulfonic acid - Wikipedia
Cu(OTf)2-Catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA)
Stereospecific synthesis of 1,5-disubstituted tetrazoles from ketoximes via a Beckmann rearrangement facilitated by diphenyl phosphorazidate - Tetrahedron Lett. - X-MOL
Hydroxylamine-O-sulfonic acid - Wikiwand
Direct and Stereospecific Synthesis of N-H and N-Alkyl Aziridines from Unactivated Olefins Using Hydroxylamine-O-Sulfonic Acids. | Semantic Scholar
Hydroxylamine-O-sulfonic acid - Wikiwand
The Beckmann fragmentation of quadricyclanone oxime - ScienceDirect
Hydroxylamine-O-sulfonic acid - WikiVisually
Table 1 from Cu(OTf)2-catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA). | Semantic Scholar
Cu(OTf)2-catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA). - Synthesis - X-MOL
Ketoxime - an overview | ScienceDirect Topics
Hydroxylamine-O-sulfonic acid - Wikipedia
Figure 1 from Cu(OTf)2-catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA). | Semantic Scholar
Hydroxylamine-O-sulfonic acid - Wikiwand
Beckmann rearrangement - Wikipedia
Direct Synthesis of Secondary Amides from Ketones through Beckmann Rearrangement using O-(Mesitylsulfonyl)hydroxylamine,Tetrahedron Letters - X-MOL
Visible-Light-Induced Beckmann Rearrangement by Organic Photoredox Catalysis.,Organic Letters - X-MOL
Synthesis of antiprotozoal diamines by regioselective insertion of nitrogen into a bicyclic ring system | SpringerLink
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)
Cu(OTf)2-Catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA)