Efficient C—N Formation for Preparing α-Branched Primary Amines by Recycled Intramolecular Reactions of 1,8-Naphthosultone Using Ammonia as Nitrogen Source-Reference-Cited by-同舟云学术

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Efficient C—N Formation for Preparing α-Branched Primary Amines by Recycled Intramolecular Reactions of 1,8-Naphthosultone Using Ammonia as Nitrogen Source

Published:2014-04 Issue:4 Volume:22 Page:405-410
ISSN:1004-9541
Container-title:Chinese Journal of Chemical Engineering
language:en
Short-container-title:Chinese Journal of Chemical Engineering

Author:

ZHOU Xinrui,CHEN Jie,ZENG Xiaoping,LIU Jihong,Istvan E. Markó

Publisher

Elsevier BV

Subject

General Chemical Engineering,General Chemistry,Biochemistry,Environmental Engineering

Reference22 articles.

1. “A straightforward route to obtain 13C1-labeled clenbuterol”;Gonzalez-Antuna;Tetrahedron,2011

2. “A new and improved process for celiprolol hydrochloride”;Joshi;Org. Process. Res. Dev.,2001

3. “Rifamycin antibiotics-new compounds and synthetic methods. Part 1: Study of the reaction of 3-formylrifamycin SV with primary alkylamines or ammonia”;Bujnowski;Tetrahedron,2003

4. “Recognition of tetramethylenedisulfotetramine and related sulfamides by the brain GABA-gated chloride channel and a cyclodiene-sensitive monoclonal antibody”;Esser;Chem. Res. Toxicol.,1991

5. “Partitioning of penoxsulam, a new sulfonamide herbicide”;Jabusch;J. Agric. Food. Chem.,2005

Cited by 1 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. DFT study on the iridium-catalyzed multi-alkylation of alcohol with ammonia;RSC Advances;2016

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