Oxidative 1,2-aryl rearrangement in flavanones using thallium(III) -tolylsulphonate (TTS)= A new useful route to isoflavones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference19 articles.
1. Recent Advances in Organothallium Chemistry
2. Applications of thallium(III) nitrate (TTN) to organic synthesis
3. Thallium(III) nitrate in organic synthesis: new experimental approaches to oxythallation
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1. Thallium(III) p-tosylate (TTS) mediated oxidative rearrangement of 2-naphthyl and 2-heteroarylchromanones;Indian Journal of Chemistry;2022-09-20
2. Novel synthesis of rotenoid, pongarotene, by oxidative rearrangement using thallium(III) p-tosylate;Synthetic Communications;2022-04-18
3. Thallium( III ) p ‐tosylate‐mediated oxidative [1,2] rearrangement of 2‐naphthyl and 2‐heteroarylchromanones;Journal of Heterocyclic Chemistry;2021-10-25
4. Scope and Applications of 2,3-Oxidative Aryl Rearrangements for the Synthesis of Isoflavone Natural Products;The Journal of Organic Chemistry;2021-07-27
5. Stille coupling for the synthesis of isoflavones by a reusable palladium catalyst in water;Journal of the Chinese Chemical Society;2021-01-20
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