Asymmetric Total Synthesis of (−)-Arborisidine and (−)-19-epi-Arborisidine Enabled by a Catalytic Enantioselective Pictet–Spengler Reaction-Reference-Cited by-同舟云学术

Asymmetric Total Synthesis of (−)-Arborisidine and (−)-19-epi-Arborisidine Enabled by a Catalytic Enantioselective Pictet–Spengler Reaction

Published:2020-07-21 Issue:33 Volume:142 Page:14276-14285
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

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 BCH5304, CH-1015 Lausanne, Switzerland

Funder

Schweizerischer Nationalfonds zur F?rderung der Wissenschaftlichen Forschung

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.0c05804

Reference88 articles.

1. Arborisidine and Arbornamine, Two Monoterpenoid Indole Alkaloids with New Polycyclic Carbon–Nitrogen Skeletons Derived from a Common Pericine Precursor

2. Arboridinine, a Pentacyclic Indole Alkaloid with a New Cage Carbon–Nitrogen Skeleton Derived from a Pericine Precursor

3. Total Synthesis of (+)-Scholarisine A

4. A Concise Total Synthesis of (+)-Scholarisine A Empowered by a Unique C–H Arylation

5. Access to the Akuammiline Family of Alkaloids: Total Synthesis of (+)-Scholarisine A

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