4.4 Article

A one-pot, two-step synthesis of 3-deazacanthin-4-ones via sequential Pd-catalyzed Suzuki-Miyaura and Cu-catalyzed Buchwald-Hartwig reactions

期刊

TETRAHEDRON LETTERS
卷 58, 期 27, 页码 2661-2664

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2017.05.076

关键词

Canthine alkaloids; Nitrogen heterocycles; Suzuki-Miyaura reaction; Buchwald-Hartwig reaction; Transition-metal catalysis

资金

  1. Erasmus+ traineeships [7069/2016]
  2. Cyprus Research Promotion Foundation [NEKYP/0308/02]

向作者/读者索取更多资源

3-Deazacanthin-4-one and nine analogues, including the 8-aza analogue, were prepared rapidly and in high yields from 8-iodoquinolones and 2-chloro(het)arylboronic acids. The strategy involves construction of the central B ring via concomitant Pd-catalyzed Suzuki-Miyaura C-C and Cu-catalyzed BuchwaldHartwig C-N coupling reactions. (C) 2017 Elsevier Ltd. All rights reserved.

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