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Direct Synthesis for Benzofuro[3,2-d]pyrimidin-2-Amines via One-Pot Cascade [4 + 2] Annulation/Aromatization between Benzofuran-Derived Azadienes and Carbodiimide Anions.
Wang, Chuan-Chuan; Wang, Qing-Long; Li, Yi-Hui; Ren, Meng-Ru; Hou, Xue-Hui; Ma, Zhi-Wei; Liu, Xue-Hua; Chen, Ya-Jing.
Afiliación
  • Wang CC; Henan University of Animal Husbandry and Economy, Faculty of Science, CHINA.
  • Wang QL; Henan University of Animal Husbandry and Economy, Faculty of Science, CHINA.
  • Li YH; Zhengzhou University, School of Pharmaceutical Sciences, CHINA.
  • Ren MR; Zhengzhou University, School of Pharmaceutical Sciences, CHINA.
  • Hou XH; Henan University of Animal Husbandry and Economy, Faculty of Science, CHINA.
  • Ma ZW; Henan University of Animal Husbandry and Economy, Faculty of Science, CHINA.
  • Liu XH; Zhengzhou University, School of Pharmaceutical Sciences, CHINA.
  • Chen YJ; Zhengzhou University, School of Pharmaceutical Sciences, 100 Science Avenue, 450001, Zhengzhou, CHINA.
Chemistry ; : e202402886, 2024 Aug 30.
Article en En | MEDLINE | ID: mdl-39212526
ABSTRACT
The chemoselective [4+2] annulation/aromatization reactions between benzofuran-derived azadienes and N-Ts cyanamides are developed, affording a convenient method for synthesizing benzofuro[3,2-d]pyrimidin-2-amines under mild conditions. Herein, N-Ts cyanamides selectively participated in reactions absolutely via carbodiimide anion intermediates and the corresponding cyanamide anion intermediates derived products were not observed. The proposed chemoselective stepwise reaction mechanism was well supported by DFT calculations.
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Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Chemistry Asunto de la revista: QUIMICA Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Chemistry Asunto de la revista: QUIMICA Año: 2024 Tipo del documento: Article