ChemInform Abstract: Photochemical and Thermal Rearrangements of 2-Arylamino-1-(4-tert-butylphenoxy)-9,10-anthraquinones.
β Scribed by I. Ya. Mainagashev; L. S. Klimenko; N. P. Gritsan
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 30 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
Photochemical and Thermal Rearrangements of 2-Arylamino-1-(4tert-butylphenoxy)-9,10-anthraquinones.
-Irradiation of the title 2-arylaminoanthraquinones (III) proceeds by migration of the tert-butylphenyl group to the 9-carbonyl oxygen to furnish 1,10-anthraquinones [as hydrolysis products (IV)] or by Smiles rearrangement to give diarylamino derivatives (V). Smiles rearrangement is also observed under basic (KOH-DMSO) or thermolysis conditions. -(MAINAGASHEV, I.
π SIMILAR VOLUMES
Heterocyclizations of 1,4-Diazido-2,3-diarylthio-9,10-anthraquinones. -Diazidoanthraquinones of type (II) undergo stepwise thermic cyclization. Under mild conditions, the phenothiazines (III) are obtained, whereas in refluxing toluene both azido groups participate in cyclizations to give oxazolo an
## 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
## 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