4.8 Article

N-substituted imines by the copper-catalyzed N-imination of boronic acids and organostannanes with O-acyl ketoximes

Journal

ORGANIC LETTERS
Volume 9, Issue 10, Pages 1947-1950

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol070561w

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Funding

  1. NCI NIH HHS [R01 CA040157-18] Funding Source: Medline
  2. NIGMS NIH HHS [GM066153, R01 GM066153-19A1, R01 GM066153] Funding Source: Medline

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Catalytic quantities of copper(I) or copper(II) sources catalyze the N-imination of boronic acids and organostannanes through reaction with oxime O-carboxylates under nonbasic conditions. This method tolerates various functional groups and takes place efficiently using aryl, heteroaryl, and alkenyl boronic acids and stannanes.

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