✦ LIBER ✦

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

✍ Scribed by Ronald J. Baumgarten; Phillip L. DeChristopher

Publisher: Elsevier Science
Year: 1967
Tongue: French
Weight: 139 KB
Volume: 8
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(00)90908-0

No coin nor oath required. For personal study only.

✦ Synopsis

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

📜 SIMILAR VOLUMES

A novel diamination: The synthesis of st

A novel diamination: The synthesis of styrene from 2-phenylethlamine via the utilization of the saccharin anion as a leaving group

✍ R.J. Baumgarten; P.J. Dechristopher 📂 Article 📅 1968 🏛 Elsevier Science 🌐 French ⚖ 36 KB

## IHOd -Hogfjp 2458 VI under the last figure should read IV'.

ChemInform Abstract: Nucleosides and Nuc

ChemInform Abstract: Nucleosides and Nucleotides. Part 165. A Novel Ring-Enlargement Reaction of (3-Oxa-2-silacyclopentyl)methyl Radicals into 4-Oxa-3-silacyclohexyl Radicals. Stereoselective Introduction of a Hydroxyethyl Group via Unusual 6-endo-Cyclization Products Derived from 3-Oxa-4-silahexenyl Radicals and Its Application to the Synthesis of a 4′-α-Branched Nucleoside.

✍ S. SHUTO; M. KANAZAKI; S. ICHIKAWA; A. MATSUDA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 39 KB 👁 2 views