A metal-free protocol for the preparation of amines using ammonia borane under mild conditions

被引:4
|
作者
Li, Xinmin [1 ,2 ]
Hu, Yue [2 ]
Alenad, Asma M. [3 ]
Zhou, Bei [2 ]
Ma, Zhuang [2 ]
Gao, Jie [2 ]
Jagadeesh, Rajenahally V. [2 ]
Beller, Matthias [2 ]
机构
[1] Zunyi Med Univ, Sch Pharm, Xuefu West Rd 6, Zunyi 563000, Peoples R China
[2] Leibniz Leibniz Inst Katalyse e V, Albert Einstein Str 29A, D-18059 Rostock, Germany
[3] Jouf Univ, Coll Sci, Chem Dept, PO Box 2014, Sakaka, Saudi Arabia
来源
ORGANIC CHEMISTRY FRONTIERS | 2023年 / 10卷 / 04期
基金
中国国家自然科学基金; 欧洲研究理事会;
关键词
CATALYZED REDUCTIVE AMINATION; SECONDARY-AMINES; FORMIC-ACID; GENERAL-SYNTHESIS; HYDROGEN; ALDEHYDES; KETONES; IRON; NITROARENES;
D O I
10.1039/d2qo01938h
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A mild and convenient reductive amination protocol for the synthesis of structurally diverse secondary and tertiary amines as well as N-methylated products under metal-free conditions is presented. This one-pot protocol works efficiently at room temperature using ammonia borane as the reductant and is applicable to a wide range of substrates, including chiral amines and amino acid derivatives. The synthetic utility and practicability of this methodology is demonstrated by gram-scale reactions and selected synthesis of current drug molecules.
引用
收藏
页码:970 / 976
页数:7
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