Brønsted Acid Promoted Thermal-Ring-Rearrangement of Fluorenopyrans to 2-(1H -Inden-3-yl)-9H -fluoren-3-ols Bearing Two All-Carbon-Quaternary Centres
Author:
Affiliation:
1. School of Chemistry; University of Hyderabad; P.O. Central University, Gachibowli 500046 Hyderabad Telangana State India
Funder
Council of Scientific and Industrial Research, India
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ejoc.202000251/fullpdf
Reference47 articles.
1. An Expeditious Benzannulation Reaction of Indol-3-yl-but-3-yn-2-ols to Substituted 2-Iodocarbazoles via Domino 5-endo Spirocyclization/Selective Vinyl Shift and Aromatization
2. Cycloisomerization of Oxindole-Derived 1,5-Enynes: A Calcium(II)-Catalyzed One-Pot, Solvent-free Synthesis of Phenanthridinones, 3-(Cyclopentenylidene)indolin-2-ones and 3-Spirocyclic Indolin-2-ones
3. Gold-Catalyzed Synthesis of 1-(Indol-3-yl)carbazoles: Selective 1,2-Alkyl vs 1,2-Vinyl Migration
4. Effect of catalyst and solvent on the furan ring rearrangement to cyclopentanone
5. Ring-rearrangement metathesis of 3,6-dialkoxy-3,6-dihydro-2H-pyrans
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