## Abstract Key steps of the title synthesis are the previously developed pyrrole acylation method with monoethyl succinate (II) and the Suzuki cross coupling reaction of 3βchloroβ6βpyrrolylpyridazine (V) with arylboronic acids.
ChemInform Abstract: The Synthesis and Chemical Reactivity of 3-Chloro-6-(2-pyrrolyl)pyridazine.
β Scribed by R. A. JONES; A. P. WHITMORE
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 32 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
The Synthesis and Chemical Reactivity of 3-Chloro-6-(2pyrrolyl)pyridazine.
-Title compound (III) is prepared and its chemical behavior is investigated in connection with studies on extended heterocyclic systems with potential semi-conductivity and non-linear optical properties. Reactions of (III) with nucleophiles are slow. The corresponding N-quaternized salt (VIII) reacts faster with nucleophiles. The introduction of a second 2-pyrrolyl substituent could not be achieved. -(JONES, R. A.;
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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 βFull Textβ option. The original article is trackable v