Iodine as a mild and versatile reagent for the synthesis of 1,3-dioxane derivatives via the Prins reaction
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference33 articles.
1. Total Synthesis of (+)-Dactylolide through an Efficient Sequential Peterson Olefination and Prins Cyclization Reaction
2. Synthesis and Antimuscarinic Activity of Derivatives of 2-Substituted-1,3-Dioxolanes
3. Formal synthesis of (+)-SCH 351448: the Prins cyclization approach
4. New 1,3-dioxolane and 1,3-dioxane derivatives as effective modulators to overcome multidrug resistance
5. The Mechanism of the Prins Reaction1
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1. Acid treated montmorillonite - efficient catalyst in Prins reaction of alpha-methylstyrene with paraldehyde;Molecular Catalysis;2023-05
2. Carbonyl and Imine Ene Reactions, Prins Reactions and Cyclizations, and Lewis Acid–Catalyzed Carbonyl Olefin Metathesis;Reference Module in Chemistry, Molecular Sciences and Chemical Engineering;2023
3. Metal-Free Synthesis of 1,3-Dioxane Derivatives from Aromatic Alkynes and Paraformaldehyde;Synlett;2022-04-12
4. Formaldehyde as C 1 Synthon in Organic Synthesis;The Chemical Transformations of C1 Compounds;2022-01-21
5. Catalysis by Halogen Bonding Based on Iodine;Iodine Catalysis in Organic Synthesis;2022-01-07
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