Synthesis of several types of 2,8-dioxabicyclo[3.3.1]nonanes using amberlyst-15 as an efficient recyclable heterogeneous catalyst
Author:
Affiliation:
1. Department of Chemistry, Jadavpur University, Kolkata, India
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/00397911.2017.1365906
Reference6 articles.
1. A Pd(ii)-catalyzed asymmetric approach toward chiral [3.3.1]-bicyclic ketals using 2-hydroxyphenylboronic acid as a pro-bis(nucleophile)
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4. Synthesis of functionalized 2-aryl-4-(indol-3-yl)-4H-chromenes via iodine-catalyzed domino Michael addition–intramolecular cyclization reaction
5. Amberlyst-15 in organic synthesis
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2. Chemistry of ( E )‐2‐(2,4‐Dioxochroman‐3‐ylidene)‐2‐phenylacetonitrile: Access to Biscoumarin‐Fused Trioxabicycles;Asian Journal of Organic Chemistry;2022-07-07
3. Switchable Synthesis of Cyclohexanedione‐fused 2,8‐Oxaza/2,8‐Dioxa Bicyclo[3.3.1]nonanes and 4‐Substituted 4 H ‐Chromenes by Tunability of the Deamination/Dehydration Process;Asian Journal of Organic Chemistry;2022-02-10
4. Controllable Synthesis of Two Isomers 4H-Chromene and 2,8-Dioxabicyclo[3.3.1]nonane Derivatives under Catalyst-Free Conditions;The Journal of Organic Chemistry;2021-11-16
5. Amberlyst 15®: An Efficient Green Catalyst for the Synthesis of Heterocyclic Compounds;Russian Journal of Organic Chemistry;2021-07
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