A New Synthesis of Indenones
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/00397917709409276
Reference11 articles.
1. A New Synthetic Route to Selected Indenones
2. The low yields of indenones may possibly be due to trapping of the intermediate radicals by the product. 5
3. Spin trapping by tetraphenylcyclopentadienone and 2,3-diarylindenones. New long-lived radicals and their relevance to benzyne promotion from benzenediazonium acetate
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1. Divergent Synthesis of α-Aroyloxy Ketones and Indenones: A Controlled Domino Radical Reaction for Di- and Trifunctionalization of Alkynes;The Journal of Organic Chemistry;2020-05-20
2. A Metal-Free Oxidative Carboannulation Approach towards Synthesis of 2,3-Diarylindenones and Its Regioisomers;ChemistrySelect;2018-02-02
3. Electrogenerated superoxide anion: Hydroxylation of electroreducible substrates in aprotic solvent;Journal of Electroanalytical Chemistry;2017-05
4. Rhodium-Catalyzed Direct Annulation of Aldehydes with Alkynes Leading to Indenones: Proceeding through in Situ Directing Group Formation and Removal;Organic Letters;2013-09-06
5. Synthesis of Diastereoisomeric 1,2,3-Triphenylindans;Australian Journal of Chemistry;1997
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