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Biomimetic Phosphate-Catalyzed Pictet-Spengler Reaction for the Synthesis of 1,1'-Disubstituted and Spiro-Tetrahydroisoquinoline Alkaloids.
Zhao, Jianxiong; Méndez-Sánchez, Daniel; Ward, John M; Hailes, Helen C.
Affiliation
  • Zhao J; Department of Chemistry , University College London , Christopher Ingold Building, 20 Gordon Street , London WC1H 0AJ , U.K.
  • Méndez-Sánchez D; Department of Chemistry , University College London , Christopher Ingold Building, 20 Gordon Street , London WC1H 0AJ , U.K.
  • Ward JM; Department of Biochemical Engineering , University College London , London WC1E 6BT , U.K.
  • Hailes HC; Department of Chemistry , University College London , Christopher Ingold Building, 20 Gordon Street , London WC1H 0AJ , U.K.
J Org Chem ; 84(12): 7702-7710, 2019 06 21.
Article in En | MEDLINE | ID: mdl-31095375
Tetrahydroisoquinoline (THIQ) alkaloids are an important group of compounds that exhibit a range of bioactivities. Here, a phosphate buffer-catalyzed Pictet-Spengler reaction (PSR) using unreactive ketone substrates is described. A variety of 1,1'-disubstituted and spiro-tetrahydroisoquinoline alkaloids were readily prepared in one-step and high yields, highlighting the general applicability of this approach. This study features the role of phosphate in the aqueous-based PSR and provides an atom-efficient, sustainable route to new THIQs.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phosphates / Spiro Compounds / Biomimetic Materials / Alkaloids / Isoquinolines Language: En Journal: J Org Chem Year: 2019 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phosphates / Spiro Compounds / Biomimetic Materials / Alkaloids / Isoquinolines Language: En Journal: J Org Chem Year: 2019 Type: Article