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dbr:Bradsher_cycloaddition
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Reacció de cicloaddició de Bradsher Bradsher cycloaddition
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La cicloaddició de Bradsher , en química, és una forma de la reacció de Diels-Alder que implica l'addició [4+2] d'un dienòfil amb aromàtics catiònics xom és l'acridizini o . La cicloaddició de Bradsher va ser donada a conèixer per C. K. Bradsher i T. W. G. Solomons en la revista Journal of the American Chemical Society de l'American Chemical Society el 1958. The Bradsher cycloaddition reaction, also known as the Bradsher cyclization reaction is a form of the Diels–Alder reaction which involves the [4+2] addition of a common dienophile with a cationic aromatic azadiene such as acridizinium or isoquinolinium. The Bradsher cycloaddition was first reported by C. K. Bradsher and T. W. G. Solomons in 1958.
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The Bradsher cycloaddition reaction, also known as the Bradsher cyclization reaction is a form of the Diels–Alder reaction which involves the [4+2] addition of a common dienophile with a cationic aromatic azadiene such as acridizinium or isoquinolinium. The Bradsher cycloaddition was first reported by C. K. Bradsher and T. W. G. Solomons in 1958. La cicloaddició de Bradsher , en química, és una forma de la reacció de Diels-Alder que implica l'addició [4+2] d'un dienòfil amb aromàtics catiònics xom és l'acridizini o . La cicloaddició de Bradsher va ser donada a conèixer per C. K. Bradsher i T. W. G. Solomons en la revista Journal of the American Chemical Society de l'American Chemical Society el 1958.
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