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Design and Applications of N-tert-Butyl Sulfinyl Squaramide Catalysts.
Li, Yao; He, Cyndi Qixin; Gao, Fei-Xiang; Li, Zhen; Xue, Xiao-Song; Li, Xin; Houk, K N; Cheng, Jin-Pei.
Afiliação
  • Li Y; State key Laboratory of Elemento-Organic Chemistry, College of Chemistry, Collaborative Innovation Center of Chemical Science and Engineering, Nankai University , Tianjin 300071, China.
  • He CQ; Department of Chemistry and Biochemistry, University of California , Los Angeles, California 90095, United States.
  • Gao FX; State key Laboratory of Elemento-Organic Chemistry, College of Chemistry, Collaborative Innovation Center of Chemical Science and Engineering, Nankai University , Tianjin 300071, China.
  • Li Z; State key Laboratory of Elemento-Organic Chemistry, College of Chemistry, Collaborative Innovation Center of Chemical Science and Engineering, Nankai University , Tianjin 300071, China.
  • Xue XS; State key Laboratory of Elemento-Organic Chemistry, College of Chemistry, Collaborative Innovation Center of Chemical Science and Engineering, Nankai University , Tianjin 300071, China.
  • Li X; State key Laboratory of Elemento-Organic Chemistry, College of Chemistry, Collaborative Innovation Center of Chemical Science and Engineering, Nankai University , Tianjin 300071, China.
  • Houk KN; Department of Chemistry and Biochemistry, University of California , Los Angeles, California 90095, United States.
  • Cheng JP; State key Laboratory of Elemento-Organic Chemistry, College of Chemistry, Collaborative Innovation Center of Chemical Science and Engineering, Nankai University , Tianjin 300071, China.
Org Lett ; 19(7): 1926-1929, 2017 04 07.
Article em En | MEDLINE | ID: mdl-28357868
A new chiral HBD system, N-tert-butyl sulfinyl squaramide, was designed and synthesized. The core N-tert-butyl sulfinyl squaramide with an 1-aminoindan-2-ol skeleton was found to be an efficient catalyst in the enantioselective Friedel-Crafts alkylation of indoles and acyl phosphonates.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article
Texto completo
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article