Coupling of α-(1H-Benzotriazol-1-yl) Nitrones with Grignard Reagents: Access to Ketonitrones
A new procedure for the synthesis of novel ketonitrones has been developed. The procedure involves the coupling of Grignard reagents with the easily accessible and stable N -substituted α-(1 H -benzotriazol-1-yl) nitrones in the presence of catalytic amounts of zinc bromide.
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Veröffentlicht in: | Russian journal of organic chemistry 2024-05, Vol.60 (5), p.950-955 |
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Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | A new procedure for the synthesis of novel ketonitrones has been developed. The procedure involves the coupling of Grignard reagents with the easily accessible and stable
N
-substituted α-(1
H
-benzotriazol-1-yl) nitrones in the presence of catalytic amounts of zinc bromide. |
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ISSN: | 1070-4280 1608-3393 |
DOI: | 10.1134/S1070428024050178 |