Synthesis of fluspidine via asymmetric NaBH4 reduction of silicon enolates of β-keto esters-Reference-Cited by-同舟云学术

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Synthesis of fluspidine via asymmetric NaBH4 reduction of silicon enolates of β-keto esters

Published:2018-09 Issue:38 Volume:74 Page:5069-5084
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Nakane Satoshi,Yoshinaka Sho,Iwase Shoutaro,Shuto Yoshihiro,Bunse Paul,Wünsch Bernhard,Tanaka Shinji,Kitamura Masato

Funder

Japan Science and Technology Agency

Ministry of Education, Culture, Sports, Science and Technology

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference55 articles.

1. Synthesis, pharmacological activity and structure affinity relationships of spirocyclic σ1 receptor ligands with a (2-fluoroethyl) residue in 3-position

2. A 18F-Labeled Fluorobutyl-Substituted Spirocyclic Piperidine Derivative as a Selective Radioligand for PET Imaging of Sigma1 Receptors

3. Synthesis, Characterization, and Metabolism Studies of Fluspidine Enantiomers

4. Current and Novel Approaches to the Drug Treatment of Schizophrenia

5. Igmesine Hydrochloride

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1. [18F]Fluspidine—A PET Tracer for Imaging of σ1 Receptors in the Central Nervous System;Pharmaceuticals;2024-01-28

2. Co(Salox)‐Catalyzed Enantioselective Reduction of α,β‐Unsaturated Esters;European Journal of Organic Chemistry;2023-02-28

3. Catalytic Asymmetric Conjugate Reduction;Angewandte Chemie International Edition;2023-02-27

4. Catalytic Asymmetric Conjugate Reduction;Angewandte Chemie;2023-02-27

5. 1,2-Carboetherification (Alkoxylation) of Olefins;Reference Module in Chemistry, Molecular Sciences and Chemical Engineering;2022

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