A new reaction of alkyl perchlorates with acetonitrile. Synthesis of N-alkylacetamides


如何引用文章

全文:

开放存取 开放存取
受限制的访问 ##reader.subscriptionAccessGranted##
受限制的访问 订阅存取

详细

An ability of n-alkyl and 1-adamantylmethyl perchlorates to be converted to the corresponding N-alkylacetamides upon treatment with acetonitrile was demonstrated. This reaction is an example of Ritter-type reaction, which proceeds under exclusively mild conditions and requires no catalysis or special activation of reagents. N-Alkylacetamides were formed in quantitative yields in analytically pure form.

作者简介

N. Yashin

Department of Chemistry, M. V. Lomonosov Moscow State University; Institute of Physiologically Active Compounds, Russian Academy of Sciences

Email: elaver@org.chem.msu.ru
俄罗斯联邦, Build. 3, 1 Leninskie Gory, Moscow, 119991; 1 Severnyi pr-d, Chernogolovka, Moscow Region, 142432

E. Averina

Department of Chemistry, M. V. Lomonosov Moscow State University; Institute of Physiologically Active Compounds, Russian Academy of Sciences; N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences

编辑信件的主要联系方式.
Email: elaver@org.chem.msu.ru
俄罗斯联邦, Build. 3, 1 Leninskie Gory, Moscow, 119991; 1 Severnyi pr-d, Chernogolovka, Moscow Region, 142432; 47 Leninsky prosp., Moscow, 119991

Yu. Grishin

Department of Chemistry, M. V. Lomonosov Moscow State University

Email: elaver@org.chem.msu.ru
俄罗斯联邦, Build. 3, 1 Leninskie Gory, Moscow, 119991

T. Kuznetsova

Department of Chemistry, M. V. Lomonosov Moscow State University

Email: elaver@org.chem.msu.ru
俄罗斯联邦, Build. 3, 1 Leninskie Gory, Moscow, 119991

N. Zefirov

Department of Chemistry, M. V. Lomonosov Moscow State University; Institute of Physiologically Active Compounds, Russian Academy of Sciences

Email: elaver@org.chem.msu.ru
俄罗斯联邦, Build. 3, 1 Leninskie Gory, Moscow, 119991; 1 Severnyi pr-d, Chernogolovka, Moscow Region, 142432

补充文件

附件文件
动作
1. JATS XML

版权所有 © Springer Science+Business Media New York, 2016