4.4 Article

Substituted pyrrole synthesis from nitrodienes

期刊

TETRAHEDRON LETTERS
卷 58, 期 23, 页码 2223-2227

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2017.04.077

关键词

Cadogan-Sundberg; Nitrodienes; Mo catalyst; Nitrene intermediate; DFT calculations

资金

  1. Petroleum Research Fund of the American Chemical Society [54244-UR4]
  2. Extreme Science and Engineering Discovery Environment (XSEDE)
  3. National Science Foundation [ACI01053575]

向作者/读者索取更多资源

Though the Cadogan-Sundberg approach has been employed to synthesize a variety of indole and carbazole derivatives from nitroarenes, surprisingly, very little is reported for making pyrroles using the same approach from non-arene nitrodienes. Herein, we report a general method to synthesize substituted pyrroles, in one step with modest yields, from nitrodienes using triphenylphosphine in the presence of an Mo catalyst, bis(acetylaceto)dioxomolybdenum (VI). To shed light on the mechanism of this reaction, we performed DFT calculations using uB3LYP/6-31+G(d) basis set and observed that the reaction favors a path through a nitrene intermediate. (C) 2017 Elsevier Ltd. All rights reserved.

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