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Synthesis of Tetrahydro-ß-carbolines by a Manganese-Catalysed Oxidative Pictet-Spengler Reaction.
Shao, Zhihui; Zhang, Xiaoyu; Li, Xinyan; Wang, Weilin; Ding, Jiaqiao; Cui, Bing; Zhao, Mingqin.
  • Shao Z; Flavors and Fragrance Engineering &, Technology Research Center of Henan Province, College of Tobacco Science, Henan Agricultural University, Zhengzhou, 450002, China.
  • Zhang X; Flavors and Fragrance Engineering &, Technology Research Center of Henan Province, College of Tobacco Science, Henan Agricultural University, Zhengzhou, 450002, China.
  • Li X; Flavors and Fragrance Engineering &, Technology Research Center of Henan Province, College of Tobacco Science, Henan Agricultural University, Zhengzhou, 450002, China.
  • Wang W; Flavors and Fragrance Engineering &, Technology Research Center of Henan Province, College of Tobacco Science, Henan Agricultural University, Zhengzhou, 450002, China.
  • Ding J; Flavors and Fragrance Engineering &, Technology Research Center of Henan Province, College of Tobacco Science, Henan Agricultural University, Zhengzhou, 450002, China.
  • Cui B; Flavors and Fragrance Engineering &, Technology Research Center of Henan Province, College of Tobacco Science, Henan Agricultural University, Zhengzhou, 450002, China.
  • Zhao M; Flavors and Fragrance Engineering &, Technology Research Center of Henan Province, College of Tobacco Science, Henan Agricultural University, Zhengzhou, 450002, China.
Chemistry ; 29(39): e202203758, 2023 Jul 11.
Article en En | MEDLINE | ID: mdl-37114329
ABSTRACT
Herein, an efficient and green procedure for the synthesis of tetrahydro-ß-carbolines via dehydrogenative coupling of alcohols with tryptamines is reported. The reaction was carried out under mild conditions in the presence of a catalytic amount of the iPr PNP-Mn catalyst and a weak base (Na2 CO3 ). This method tolerated a variety of benzylic and aliphatic alcohol substrates with different functional groups and afforded diverse products in good to excellent isolated yields using tryptamines. Using this strategy, we successfully synthesised pharmaceutical molecules harman, harmaline, and harmine in a concise manner.
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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2023 Tipo del documento: Article