Enantioselective Synthesis of 1-Aryl-Substituted Tetrahydroisoquinolines Through Ru-Catalyzed Asymmetric Transfer Hydrogenation
Author:
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ejoc.201500951/fullpdf
Reference139 articles.
1. The Chemistry and Biology of Isoquinoline Alkaloids
2. Chemistry and Biology of the Tetrahydroisoquinoline Antitumor Antibiotics
3. β-Phenylethylamines and the isoquinoline alkaloids
4. Simple indole alkaloids and those with a nonrearranged monoterpenoid unit
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1. Enantiodivergent Synthesis of 1-Heteroaryl Tetrahydroisoquinolines Catalyzed by Imine Reductases;Organic Letters;2023-04-03
2. Chiral 8-Amino-5,6,7,8-tetrahydroquinoline Derivatives in Metal Catalysts for the Asymmetric Transfer Hydrogenation of 1-Aryl Substituted-3,4-dihydroisoquinolines as Alkaloids Precursors;Molecules;2023-02-16
3. Introduction of chirality at C1 position of 1-substituted-3,4-dihydroisoquinoline by its enantioselective reduction: synthesis of chiral 1-substituted-1,2,3,4-tetrahydroisoquinoline – a review;RSC Advances;2023
4. Application of Rh(I)/Bicyclo[2.2.1]heptadiene Catalysts to the Enantioselective Synthesis of Chiral Amines;The Chemical Record;2021-10
5. Diastereospecific Synthesis of Tetrahydroisoquinolines via Radical Cyclization: Application in the Synthesis of ent‐Tadalafil;Advanced Synthesis & Catalysis;2021-07-06
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