"1368"^^ . . . . . . . . . "La cicloaddici\u00F3 de Bradsher , en qu\u00EDmica, \u00E9s una forma de la reacci\u00F3 de Diels-Alder que implica l'addici\u00F3 [4+2] d'un dien\u00F2fil amb arom\u00E0tics cati\u00F2nics xom \u00E9s l'acridizini o . La cicloaddici\u00F3 de Bradsher va ser donada a con\u00E8ixer 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."@ca . . . . "The Bradsher cycloaddition reaction, also known as the Bradsher cyclization reaction is a form of the Diels\u2013Alder 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."@en . . . "34372981"^^ . . . . . . . . . . . . . "Reacci\u00F3 de cicloaddici\u00F3 de Bradsher"@ca . . . . . . "The Bradsher cycloaddition reaction, also known as the Bradsher cyclization reaction is a form of the Diels\u2013Alder 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."@en . "La cicloaddici\u00F3 de Bradsher , en qu\u00EDmica, \u00E9s una forma de la reacci\u00F3 de Diels-Alder que implica l'addici\u00F3 [4+2] d'un dien\u00F2fil amb arom\u00E0tics cati\u00F2nics xom \u00E9s l'acridizini o . La cicloaddici\u00F3 de Bradsher va ser donada a con\u00E8ixer 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."@ca . . . "1061404171"^^ . . . . "Bradsher cycloaddition"@en . . . . . . .