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
- DOI
- 10.1002/jlcr.511
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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.
📜 SIMILAR VOLUMES
## 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