4.4 Article

Efficient and convenient synthesis of spiroindolinone-quinazolines induced by stannous chloride

期刊

TETRAHEDRON
卷 67, 期 48, 页码 9342-9346

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2011.09.130

关键词

Quinazoline; Spirooxindole derivatives; Synthesis; Stannous chloride

资金

  1. Foundation of the Natural Science Foundation of China [21072144]
  2. Natural Science Foundation of the Jiangsu Higher Education Institutions [10KJA150049]
  3. Priority Academic Project Development of Jiangsu Higher Education Institutions
  4. Foundation of Key Laboratory of Organic Synthesis of Jiangsu Province [JSK0812]

向作者/读者索取更多资源

An efficient, convenient, one-pot synthesis of 1'H-spiro[indoline-3,2'-quinazoline]-2,4'(3'H)-dione derivatives was accomplished in good yields via the novel reductive cyclization of 2-nitrobenzamides and isatins mediated by SnCl2 center dot 2H(2)O system. A variety of substrates can participate in the process with good yields, making this methodology have broad applicability. The structure of compound 3c has been confirmed by X-ray diffraction analysis. (C) 2011 Published by Elsevier Ltd.

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