The characteristic mass spectrometric fragmentation patterns of sterically congested stilbenes, phenyl-substituted 2,2,5,5-tetramethyl-3,4-diphenylhex-3-enes, are described. In contrast to stilbene, these sterically congested stilbenes show facile loss of tert-butyl and/or isobutene and phenyl, ulti
β¦ LIBER β¦
Effects of para-Phenyl Group on the Reactivities of Sterically Congested Triplet Diphenylcarbene.
β Scribed by Katsuyuki Hirai; Takashi Iikubo; Hideo Tomioka
- Publisher
- John Wiley and Sons
- Year
- 2003
- Weight
- 107 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
Abstract
For Abstract see ChemInform Abstract in Full Text.
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