Synthesis of a Stable Primary-Alkyl-Substituted Selenenyl Iodide and Its Hydrolytic Conversion to the Corresponding Selenenic Acid
A primary-alkyl-substituted selenenyl iodide was successfully synthesized through oxidative iodination of a selenol with N-iodosuccinimide by taking advantage of a cavity-shaped steric protection group. The selenenyl iodide exhibited high thermal stability and remained unchanged upon heating at 100...
Main Authors: | Shohei Sase, Ryo Kakimoto, Ryutaro Kimura, Kei Goto |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2015-12-01
|
Series: | Molecules |
Subjects: | |
Online Access: | http://www.mdpi.com/1420-3049/20/12/19773 |
Similar Items
-
Demonstration of the Formation of a Selenocysteine Selenenic Acid through Hydrolysis of a Selenocysteine Selenenyl Iodide Utilizing a Protective Molecular Cradle
by: Kei Goto, et al.
Published: (2023-12-01) -
Effect of thimerosal on thyroid hormones metabolism in rats
by: Thiago U Pantaleão, et al.
Published: (2017-11-01) -
The many faces of thyroxine
by: Mary B. Dratman, et al.
Published: (2020-05-01) -
Sub-5 nm Gate-Length Monolayer Selenene Transistors
by: Qiang Li, et al.
Published: (2023-07-01) -
The Physiological Functions and Polymorphisms of Type II Deiodinase
by: Yan Deng, et al.
Published: (2023-04-01)