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Effective Syntheses of 2-trimethylsilylmethyl-3-trimethylsilyl-1-propene and its 1,1-d2- and 1,1,1′,1′,3,3- d6-isotopomers

✍ Scribed by Jun Hu; Robert R. Squires


Publisher
John Wiley and Sons
Year
2001
Tongue
French
Weight
92 KB
Volume
44
Category
Article
ISSN
0022-2135

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✦ Synopsis


Abstract

New and effective routes to synthesize 2‐trimethylsilylmethyl‐3‐trimethylsilyl‐1‐propene and its 1,1‐d~2~‐ and 1,1,1′,1′,3,3‐d~6~‐isotopomers have been developed, using the displacement reaction of lithium trimethylsilylcyanocuprate with allylic halides and tosylates. These compounds are pivotal precursors for the gas‐phase synthesis and characterization of the trimethylenemethane anion, and for negative ion photoelectron spectroscopic investigations of the singlet–triplet splitting in trimethylenemethane. Copyright © 2001 John Wiley & Sons, Ltd.


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Formation of 1,1,2,3,3-pentakis(arylthio
✍ Noboru Matsumura; Yasuyo Shimizu; Yoshio Yagyu; Hiroo Inoue; Kazuhiko Mizuno; To 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 257 KB 👁 1 views

## The reaction of tetrachlorocyclopropene (1) with arenethiols (2a-e), followed by treatment with perchloric acid, gave tris(arylthio)cyclopropenylium perchlorates (3a-c and e), 1,1,2,3,3-pentakis(arylthio)-1-propenes (4a-d), and 2,3,3tris(arylthio)propenals (5a-d). The structures of tris(phenylth