The Relativecis/transReactivity in the Hydrochlorination of 1-Arylpropenes
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/47/6/47_6_1477/_pdf
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4. Polar additions to olefins and acetylenes. VI. Nonstereospecific addition of bromine to 1-phenylpropene and trans-anethole
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1. Stereochemistry and Mechanism of the Brønsted Acid Catalyzed Intramolecular Hydrofunctionalization of an Unactivated Cyclic Alkene;Chemistry – A European Journal;2011-04-19
2. 2 Hydrogen-NMR. Coupling constant. Substance no. 3478ff;Landolt-Börnstein - Group III Condensed Matter;2000
3. 2 Hydrogen-NMR. Coupling constant. References;Landolt-Börnstein - Group III Condensed Matter;2000
4. Influence of alkene structure on the formation constants of alkene–ICl molecular complexes;Canadian Journal of Chemistry;1986-11-01
5. Structure and reactivity of .alpha.,.beta.-unsaturated ethers. XV. Acid-Catalyzed hydrolysis of alkyl propenyl ethers. Relative cis/trans reactivity;The Journal of Organic Chemistry;1974-10
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