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Novel deamination. II. Synthesis of styrene and trans-stilbene from 2-phenylethylamine and N-(1,2-diphenylethyl) amine via the utilization of amide and imide anions as leaving groups

✍ Scribed by Baumgarten, Ronald J.

Book ID: 120523728
Publisher: American Chemical Society
Year: 1968
Tongue: English
Weight: 484 KB
Volume: 33
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo01265a046

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A novel deamination: The synthesis of st

A novel deamination: The synthesis of styrene from 2-phenylethyl amine via the utilization of the saccharin anion as a leaving group.

✍ Ronald J. Baumgarten; Phillip L. DeChristopher 📂 Article 📅 1967 🏛 Elsevier Science 🌐 French ⚖ 139 KB

Dehydrowlatious are commonly accomplished via nucleophlllic substitutions and elimln-atious on derivatives such as the tosyl esters of the parent alcohols. Groups such as the