Reactivities of Stable Rotamers. XVIII. Reactions of 9-[2-(1-Hydroxyethyl)-1-naphthyl]fluorene Rotamers with Sulfuric Acid and Thionyl Chloride
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/60/1/60_1_223/_pdf
Reference22 articles.
1. Reactivities of Stable Rotamers. X. Reactions of 9-(2-Formyl-1-naphthyl)fluorene Rotamers and Related Compounds
2. Reactivities of Stable Rotamers. XII. Reactions of 9-(2-Bromomethyl-6-methylphenyl)fluorene Rotamers with Nucleophiles
3. Contrasting Behavior in the Substitution Reactions of 9-(2-Bromomethyl-6-methylphenyl)fluorene Rotamers
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1. A highly diastereoselective tandem Michael-Michael addition reaction in a rotameric ring system: steric acceleration due to conformation locking;Tetrahedron;1993-01
2. Reactivity of Rotational Isomers;Reactivity and Structure Concepts in Organic Chemistry;1993
3. Bromine Addition to Rotameric 1-(9-Fluorenyl)-2-(1-methylvinyl)naphthalene. Fate of Intermediate Cations Produced by Bromine Cation Attack;Chemistry Letters;1991-04
4. Reactivities of Stable Rotamers. XIX. Basicities of Rotameric 9-[2-(Dialkylaminomethyl)-6-methylphenyl]fluorenes and Solvent Effects on Them;Bulletin of the Chemical Society of Japan;1987-02
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