Direct Reductive Amination of Aldehydes Using Hantzsch Ester Promoted by N,N′ ‐Diphenyl‐ S ‐Benzylisothiouronium Iodide as an Organocatalyst
Author:
Affiliation:
1. School of Chemical Engineering, College of EngineeringChonnam National University Gwangju 61186 Republic of Korea
Funder
Basic Science Research Program through the National Research Foundation of Korea funded by the Ministry of Education
Publisher
Wiley
Subject
General Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/bkcs.11863
Reference42 articles.
1. Recent Development on Catalytic Reductive Amination and Applications
2. Approaching Highly Enantioselective Reductive Amination
3. Aldo-X Bifunctional Building Blocks for the Synthesis of Heterocycles
4. Reductive alkylation of dimethylamine using titanium(IV) isopropoxide and sodium borohydride: an efficient, safe, and convenient method for the synthesis of N,N-dimethylated tertiary amines.
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Chiral Proline Amide‐Isothiouronium Salt Spaced with Diamine as an Efficient Bifunctional Organocatalyst for Enantioselective α‐Hydrazination of Aldehydes;ChemistrySelect;2023-04-04
2. S ‐Benzyl‐ N,N′ ‐diphenyl Isothiouronium Iodide as an Efficient Organocatalyst for the Transfer Hydrogenation of 1,4‐Benzoxazines;ChemistrySelect;2022-01-25
3. S-Benzyl-N,N'-diphenyl substituted isothiouronium iodide as a highly efficient organocatalyst for transfer hydrogenation of 2-substituted quinolines;Tetrahedron Letters;2021-11
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