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• W2110364549 startingPage "9060" @default.
• W2110364549 abstract "o-Bromo(propa-1,2-dien-1-yl)arenes exhibit novel and orthogonal reactivity under Pd catalysis in the presence of secondary amines to form enamines (concerted Pd insertion, intramolecular carbopalladation, and terminative Buchwald–Hartwig coupling) and of amides to form indoles (addition, Buchwald–Hartwig cyclization, and loss of the acetyl group). The substrates for these reactions can be accessed in a reliable and highly selective two-step process from 2-bromoaryl bromides." @default.
• W2110364549 created "2016-06-24" @default.
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• W2110364549 date "2011-10-13" @default.
• W2110364549 modified "2023-09-28" @default.
• W2110364549 title "<i>ortho</i>-Bromo(propa-1,2-dien-1-yl)arenes: Substrates for Domino Reactions" @default.
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• W2110364549 doi "https://doi.org/10.1021/jo201679s" @default.
• W2110364549 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/21958309" @default.
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