Group-assisted Purification (GAP) Chemistry/Technology in Synthesizing the Chiral Intermediate of Rivastigmine and Its α-Alkyl Benzylamine Analogues-Reference-Cited by-同舟云学术

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Group-assisted Purification (GAP) Chemistry/Technology in Synthesizing the Chiral Intermediate of Rivastigmine and Its α-Alkyl Benzylamine Analogues

Published:2019-09-05 Issue:9 Volume:48 Page:1065-1068
ISSN:0366-7022
Container-title:Chemistry Letters
language:en
Short-container-title:Chem. Lett.

Author:

Yang Bing¹²,Zhang Chun-Yan³,Xu Jing²,Zheng Da-Jun²,Wang Xiao-Ying²,Dai Hong¹,Shi Yu-Jun¹,Zhu Hai-Liang²

Affiliation:

1. School of Chemistry and Chemical Engineering, Nantong University, Nantong 226019, P. R. China

2. Institute of Chemistry and Biomedical Science, State Key Laboratory of Pharmaceutical Biotechnology, Nanjing University, Nanjing 210023, P. R. China

3. Department of Pharmacy, Affiliated Hospital of Nantong University, Nantong 226001, P. R. China

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

http://www.journal.csj.jp/doi/pdf/10.1246/cl.190288

Reference40 articles.

1. A reductive aminase from Aspergillus oryzae

2. Mapping the substrate scope of monoamine oxidase (MAO-N) as a synthetic tool for the enantioselective synthesis of chiral amines

3. Stereospecific Nucleophilic Substitution of Enantioenriched Tertiary Benzylic Amines via in Situ Activation with Benzyne

4. Rivastigmine: an update on therapeutic efficacy in Alzheimer's disease and other conditions

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1. Saturated Heterocycles as Chiral Auxiliaries;Chiral Building Blocks in Asymmetric Synthesis;2022-08-12

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