4.4 Article

Approach to highly functionalized oxazolones by a Pd-catalyzed cyclization of N-alkynyl tert-butyloxycarbamates

Journal

TETRAHEDRON LETTERS
Volume 53, Issue 27, Pages 3433-3436

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2012.04.074

Keywords

Oxazolones; N-Alkynyl tert-butyloxycarbamates; Palladium; Oxypalladation; Allyl halides

Funding

  1. National Natural Science Foundation of China [20902084, 21172199]
  2. Analysis and Testing Project of Zhejiang Province [2011C37051]

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A mild and operationally simple approach to highly functionalized oxazolones has been developed, which involves an intramolecular oxypalladation of N-alkynyl tert-butyloxycarbamates, followed by either protonolysis of the alkenyl C-Pd bond to afford 3,5-disubstituted oxazolones or allylation with allyl halides in the presence of Ag2CO3 to generate 3,4,5-trisubstituted oxazolones, respectively. (C) 2012 Elsevier Ltd. All rights reserved.

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