An efficient and atom-economical route to N-aryl amino alcohols from primary amines-Reference-Cited by-同舟云学术

An efficient and atom-economical route to N-aryl amino alcohols from primary amines

Published:2018 Issue:60 Volume:8 Page:34304-34308
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Xiao Zhen¹²³⁴,Li Juanjuan¹²³⁴,Yue Qiang¹²³⁴,Zhang Qian¹²³⁴,Li Dong¹²³⁴⁵^ORCID

Affiliation:

1. School of Materials and Chemical Engineering

2. Hubei University of Technology

3. Wuhan 430068

4. China

5. Hubei Key Laboratory of Drug Synthesis and Optimization

Abstract

A novel method for generation of N-aryl amino alcohols from N,N-disubstituted picolinamides through reduction/ring-opening reaction with NaBH₄ was developed.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/RA/C8RA07355D

Reference23 articles.

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2. Amino alcohol effects on the ruthenium(II)-catalysed asymmetric transfer hydrogenation of ketones in propan-2-ol

3. Enantioselective Henry Reactions under Dual Lewis Acid/Amine Catalysis Using Chiral Amino Alcohol Ligands

4. Antagonists of the Calcium Receptor I. Amino Alcohol-Based Parathyroid Hormone Secretagogues

5. Solvent-free copper-catalyzed N-arylation of amino alcohols and diamines with aryl halides

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