Cross-Coupling Reaction of Chloropyridazines and Grignard Reagents with Nickel-phosphine Complexes : Alkylation and Arylation of Pyridazines
Alkyl- and arylpyridazines have been prepared by cross-coupling reaction between chloropyridazines and Grignard reagents in the presence of nickel-phosphine complexes (as catalysts). Hitherto unaccessible naphthyl- and thienylpyridazines have been obtained.
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Published in: | Chemical & pharmaceutical bulletin Vol. 26; no. 8; pp. 2550 - 2554 |
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Main Authors: | , , |
Format: | Journal Article |
Language: | English |
Published: |
The Pharmaceutical Society of Japan
1978
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Subjects: | |
Online Access: | Get full text |
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Summary: | Alkyl- and arylpyridazines have been prepared by cross-coupling reaction between chloropyridazines and Grignard reagents in the presence of nickel-phosphine complexes (as catalysts). Hitherto unaccessible naphthyl- and thienylpyridazines have been obtained. |
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ISSN: | 0009-2363 1347-5223 |
DOI: | 10.1248/cpb.26.2550 |