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Synthesis and reactivity of heterocyclic hydroxylamine-O-sulfonates in: Heterocyclic Communications Volume 20 Issue 3 (2014)
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Direct and Stereospecific Synthesis of N-H and N-Alkyl Aziridines from Unactivated Olefins Using Hydroxylamine-O-Sulfonic Acids. | Semantic Scholar
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Figure 1 from Cu(OTf)2-catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA). | Semantic Scholar
![Table 1 from Cu(OTf)2-catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA). | Semantic Scholar Table 1 from 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)
Table 1 from Cu(OTf)2-catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA). | Semantic Scholar
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Synthesis of a tricyclic lactam via Beckmann rearrangement and ring-rearrangement metathesis as key steps. - Abstract - Europe PMC
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Visible-Light-Induced Beckmann Rearrangement by Organic Photoredox Catalysis.,Organic Letters - X-MOL
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Dichloroimidazolidinedione-Activated Beckmann Rearrangement of Ketoximes for Accessing Amides and Lactams - J. Org. Chem. - X-MOL
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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)
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Stereospecific synthesis of 1,5-disubstituted tetrazoles from ketoximes via a Beckmann rearrangement facilitated by diphenyl phosphorazidate - Tetrahedron Lett. - X-MOL
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Direct Synthesis of Secondary Amides from Ketones through Beckmann Rearrangement using O-(Mesitylsulfonyl)hydroxylamine,Tetrahedron Letters - X-MOL
![Synthesis and reactivity of heterocyclic hydroxylamine-O-sulfonates in: Heterocyclic Communications Volume 20 Issue 3 (2014) Synthesis and reactivity of heterocyclic hydroxylamine-O-sulfonates in: Heterocyclic Communications Volume 20 Issue 3 (2014)](https://www.degruyter.com/view/journals/hc/20/3/graphic/hc-2014-0050_scheme6.jpg)