An efficient method for the oxathioacetalization of carbonyl compounds using N-bromosaccharin as a catalyst
Author:
Publisher
Elsevier BV
Subject
General Chemistry
Reference20 articles.
1. A highly efficient procedure for the oxathioacetalization of carbonyl compounds under solvent-free conditions
2. Asymmetric syntheses based on 1,3-oxathianes. 1. Scope of the reaction
3. Facile synthesis of 1,3-oxathiolanes from ketones and i-mercaptoethanol
4. Cyclopentane synthesis and annulation: Intramolecular radical cyclization of acetals
5. Anhydrous lanthanum trichloride, a mild and convenient reagent for thioacetalization
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1. Versatile Quinazolinone Synthesis: N‐Bromosaccharin‐Catalyzed Divergence in 2,3‐Dihydroquinazolin‐4(1H)‐one and Quinazolin‐4(3H)‐one Formation;ChemistrySelect;2024-03-19
2. Blue LED-Promoted Oxathiacetalization of Aldehydes and Ketones;European Journal of Organic Chemistry;2020-04-21
3. Artificial sugar saccharin and its derivatives: role as a catalyst;RSC Advances;2020
4. Recent advances in the application of acetophenone in heterocyclic compounds synthesis;Journal of the Iranian Chemical Society;2019-10-23
5. 1,3-Oxathia-, 1,3-Dioxa- and 1,3-Dithiolanes from ?,?-Unsaturated Aldehydes;Mini-Reviews in Organic Chemistry;2016-07-20
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