Catalytic Enantioselective Pictet–Spengler Reaction of α‐Ketoamides Catalyzed by a Single H‐Bond Donor Organocatalyst-Reference-Cited by-同舟云学术

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Catalytic Enantioselective Pictet–Spengler Reaction of α‐Ketoamides Catalyzed by a Single H‐Bond Donor Organocatalyst

Published:2022-03-11 Issue:19 Volume:134 Page:
ISSN:0044-8249
Container-title:Angewandte Chemie
language:en
Short-container-title:Angewandte Chemie

Author:

Andres Rémi¹,Wang Qian¹,Zhu Jieping¹^ORCID

Affiliation:

1. Laboratory of Synthesis and Natural Products Institute of Chemical Sciences and Engineering Ecole Polytechnique Fédérale de Lausanne, EPFL-SB-ISIC-LSPN, BCH 5304, 1015 Lausanne Switzerland

Funder

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ange.202201788

Reference71 articles.

1. β-Carboline alkaloid monomers and dimers: Occurrence, structural diversity, and biological activities

3. Über die Bildung von Isochinolin‐derivaten durch Einwirkung von Methylal auf Phenyl‐äthylamin, Phenyl‐alanin und Tyrosin

4. The Pictet-Spengler Reaction in Nature and in Organic Chemistry

5. Die Pictet-Spengler-Reaktion in der Natur und der organischen Chemie

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1. Divergent Asymmetric Total Synthesis of (−)‐Voacafricines A and B;Angewandte Chemie International Edition;2023-03-13

2. Divergent Asymmetric Total Synthesis of (−)‐Voacafricines A and B;Angewandte Chemie;2023-03-13

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