![Cu(OTf)2-catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA). - Abstract - Europe PMC Cu(OTf)2-catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA). - Abstract - Europe PMC](https://europepmc.org/articles/PMC7367085/bin/nihms-1567154-f0006.jpg)
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 The Mechanochemical Beckmann Rearrangement: An Eco-efficient “Cut-and-Paste” Strategy to Design the “Good Old Amide Bond” | ACS Sustainable Chemistry & Engineering](https://pubs.acs.org/cms/10.1021/acssuschemeng.0c07254/asset/images/large/sc0c07254_0003.jpeg)
The Mechanochemical Beckmann Rearrangement: An Eco-efficient “Cut-and-Paste” Strategy to Design the “Good Old Amide Bond” | ACS Sustainable Chemistry & Engineering
Regioselective Functionalization. 6.1 Migratory Preferences in Hydroxylamine-O-sulfonic Acid and Schmidt Rearrangements of 7-Substituted Norcamphors | The Journal of Organic Chemistry
![New insights into synthesis and oligomerization of ε-lactams derived from the terpenoid ketone (−)-menthone - RSC Advances (RSC Publishing) DOI:10.1039/C5RA15656D New insights into synthesis and oligomerization of ε-lactams derived from the terpenoid ketone (−)-menthone - RSC Advances (RSC Publishing) DOI:10.1039/C5RA15656D](https://pubs.rsc.org/image/article/2015/RA/c5ra15656d/c5ra15656d-s1_hi-res.gif)
New insights into synthesis and oligomerization of ε-lactams derived from the terpenoid ketone (−)-menthone - RSC Advances (RSC Publishing) DOI:10.1039/C5RA15656D
![Cu(OTf)2-catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA). - Abstract - Europe PMC Cu(OTf)2-catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA). - Abstract - Europe PMC](https://europepmc.org/articles/PMC7367085/bin/nihms-1567154-f0005.jpg)
Cu(OTf)2-catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA). - Abstract - Europe PMC
![Cu(OTf)2-catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA). - Abstract - Europe PMC Cu(OTf)2-catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA). - Abstract - Europe PMC](https://europepmc.org/articles/PMC7367085/bin/nihms-1567154-t0002.jpg)
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 The Mechanochemical Beckmann Rearrangement: An Eco-efficient “Cut-and-Paste” Strategy to Design the “Good Old Amide Bond” | ACS Sustainable Chemistry & Engineering](https://pubs.acs.org/cms/10.1021/acssuschemeng.0c07254/asset/images/medium/sc0c07254_0015.gif)
The Mechanochemical Beckmann Rearrangement: An Eco-efficient “Cut-and-Paste” Strategy to Design the “Good Old Amide Bond” | ACS Sustainable Chemistry & Engineering
![Cu(OTf)2-catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA). - Abstract - Europe PMC Cu(OTf)2-catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA). - Abstract - Europe PMC](https://europepmc.org/articles/PMC7367085/bin/nihms-1567154-f0003.jpg)
Cu(OTf)2-catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA). - Abstract - Europe PMC
![One‐Pot Synthesis of Diazirines and 15N2‐Diazirines from Ketones, Aldehydes and Derivatives: Development and Mechanistic Insight - Ibert - 2021 - Advanced Synthesis & Catalysis - Wiley Online Library One‐Pot Synthesis of Diazirines and 15N2‐Diazirines from Ketones, Aldehydes and Derivatives: Development and Mechanistic Insight - Ibert - 2021 - Advanced Synthesis & Catalysis - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/c2016368-3b8e-4e51-8548-5e28b5834a0d/adsc202100679-fig-5005-m.jpg)