Chemical Reduction and Dimerization of 1-Chloro-2,3,4,5-tetraphenylborole
✍ Scribed by Prof. Dr. Holger Braunschweig; Dr. Ching-Wen Chiu; Johannes Wahler; Dr. Krzysztof Radacki; Dr. Thomas Kupfer
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 301 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0947-6539
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Chloroformylation of 5,5-dimethyl-1,2- oxathiolan-4-one 2,2-dioxide 4 with Vilsmeier reagent (DMF/POCl 3 ) led to the formation of cyclic β-chlorovinylaldehyde (4-chloro-5,5-dimethyl-3-formyl-1,2oxathiolene 2,2-dioxide 5). Compound 5 reacted with formamidine, o-aminophenol, 1,2-phenylenediamine, ami
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## 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 “Full Text” option. The original article is trackable v