Synthesis of 4(5)-[5-(Aminomethyl)tetrahydrofuran-2-yl- or 5-(Aminomethyl)-2,5-dihydrofuran-2-yl]imidazoles by Efficient Use of a PhSe Group: Application to Novel Histamine H3-Ligands1-Reference-Cited by-同舟云学术

Synthesis of 4(5)-[5-(Aminomethyl)tetrahydrofuran-2-yl- or 5-(Aminomethyl)-2,5-dihydrofuran-2-yl]imidazoles by Efficient Use of a PhSe Group: Application to Novel Histamine H3-Ligands1

Published:1999-10-16 Issue:23 Volume:64 Page:8608-8615
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Harusawa Shinya¹,Imazu Tomonari¹,Takashima Seiichiroh¹,Araki Lisa¹,Ohishi Hirofumi¹,Kurihara Takushi¹,Sakamoto Yasuhiko¹,Yamamoto Yumiko¹,Yamatodani Atsushi¹

Affiliation:

1. Osaka University of Pharmaceutical Sciences, 4-20-1 Nasahara, Takatsuki, Osaka 569-1094, Japan, R&D Division, AZWELL, Inc., 2-24-3, Sho, Ibaraki, Osaka 567-0806, Japan, and School of Allied Health Sciences, Faculty of Medicine, Osaka University, 1-7 Yamadaoka, Suita, Osaka 565-0871, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo9910637

Reference36 articles.

1. Synthesis of imifuramine and its stereoisomers exhibiting histamine H3-agonistic activity

2. Three loci related to the src oncogene and tyrosine-specific protein kinase activity in Drosophila

3. Highly potent and selective ligands for histamine H3-receptors

4. Is the histaminergic neuron system a regulatory center for whole-brain activity?

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