ChemInform Abstract: Thermally Induced Cyclodehydrogenation of Biaryls: A Simple Radical Reaction or a Sequence of Rearrangements?
β Scribed by J. CIOSLOWSKI; P. PISKORZ; D. MONCRIEFF
- Book ID
- 101866102
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 26 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
Thermally Induced Cyclodehydrogenation of Biaryls: A Simple Radical Reaction or a Sequence of Rearrangements?
-The first direct radical pathway from 1-phenylnaphthalene to fluoranthene predominates at lower temperatures. The second pathway involves an arylaryne/anellated cyclopentadienylidenecarbene mechanism. The third pathway involves direct equilibration and is associated with very high activation energies, so that an operation under normal pyrolytic conditions is not probable. -(CIOSLOWSKI,
π SIMILAR VOLUMES
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
## A Practical Modification of the Barton-McCombie Reaction and Radical O-to S-Rearrangement of Xanthates. -A novel method for the title reaction avoiding toxic or expensive reagents is presented. It is noteworthy that in benzene as solvent the O-to S-rearranged compound is the major product. -(
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v