Enantioselective Pictet–Spengler Reaction of Acyclic α-Ketoesters Using Chiral Imidazoline-Phosphoric Acid Catalysts-Reference-Cited by-同舟云学术

Enantioselective Pictet–Spengler Reaction of Acyclic α-Ketoesters Using Chiral Imidazoline-Phosphoric Acid Catalysts

Published:2022-01-26 Issue:4 Volume:24 Page:1072-1076
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Nakamura Shuichi¹²^ORCID,Matsuda Yoichiro²,Takehara Tsunayoshi³^ORCID,Suzuki Takeyuki³^ORCID

Affiliation:

1. Department of Life Science and Applied Chemistry, Graduate School of Engineering, Nagoya Institute of Technology, Gokiso, Showa-ku, Nagoya 466-8555, Japan

2. Department of Frontier Materials, Graduate School of Engineering, Nagoya Institute of Technology, Gokiso, Showa-ku, Nagoya 466-8555, Japan

3. The Institute of Scientific and Industrial Research, Osaka University, 8-1 Mihogaoka, Ibaraki-shi, Osaka 567-0047, Japan

Funder

Astellas Foundation for Research on Metabolic Disorders

Takahashi Industrial and Economic Research Foundation

Shiono Wellness Foundation

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.1c04316

Reference56 articles.

1. Pharmacological Importance of Optically Active Tetrahydro-β-carbolines and Synthetic Approaches to Create the C1 Stereocenter

2. Spiroindolones, a Potent Compound Class for the Treatment of Malaria

3. First Asymmetric Total Syntheses of (−)-Subincanadines A and B, Skeletally Rearranged Pentacyclic Monoterpenoid Indole Alkaloids in Aspidosperma subincanum

4. Subincanadines A−C, Novel Quaternary Indole Alkaloids from Aspidosperma subincanum

5. (±)-Peharmaline A: A Pair of Rare β-Carboline-Vasicinone Hybrid Alkaloid Enantiomers from Peganum harmala

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