Reaction of Selenoamide Dianions with Thio- and Selenoformamides Leading to the Formation of 5-Aminoselenazoles: Photophysical and Electrochemical Properties-Reference-Cited by-同舟云学术

Reaction of Selenoamide Dianions with Thio- and Selenoformamides Leading to the Formation of 5-Aminoselenazoles: Photophysical and Electrochemical Properties

Published:2014-05-06 Issue:11 Volume:79 Page:4930-4939
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Murai Toshiaki¹²,Yamaguchi Kirara¹,Hori Fumihiko¹,Maruyama Toshifumi¹

Affiliation:

1. Department of Chemistry and Biomolecular Science, Faculty of Engineering, Gifu University, Yanagido, Gifu 501-1193, Japan

2. JST, ACT-C, 4-1-8 Honcho, Kawaguchi, Saitama 332-0012, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo500499g

Reference78 articles.

1. An Efficient Access to Selenazoline-4-Carboxylate Derivatives Incorporating Cyclopropyl Groups

2. Synthesis of 4-Aryl-2-imino-2H-selenazolines by a Reaction of α α-(Selenocyanato)acetophenones With Anilines

3. Reactivity of chlorodeoxypseudoephedrines with oxo-, thio-, and selenocyanates

4. Possible new organoselenium supplement – evaluation of its influence on the kidneys in comparison with inorganic sodium selenite

5. OGA inhibition by GlcNAc-selenazoline

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