Facile, regioselective oxidative selenocyanation of N-aryl enaminones under transition-metal-free conditions
Author:
Affiliation:
1. Department of Post-Graduate Studies and Research in Chemistry Mangalore University
2. Mangalgangothri-574199
3. India
Abstract
The present selenocyanation is applied for the synthesis of selenocyanated chromones, indoles and anilines in good to excellent yields.
Funder
Science and Engineering Research Board
Publisher
Royal Society of Chemistry (RSC)
Subject
Materials Chemistry,General Chemistry,Catalysis
Link
http://pubs.rsc.org/en/content/articlepdf/2020/NJ/C9NJ05845A
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3. Simultaneous Targeting of COX-2 and AKT Using Selenocoxib-1-GSH to Inhibit Melanoma
4. 1,4-Phenylenebis(Methylene)Selenocyanate, but Not Selenomethionine, Inhibits Androgen Receptor and Akt Signaling in Human Prostate Cancer Cells
5. Comparative effects of phenylenebis(methylene)selenocyanate isomers on xenobiotic metabolizing enzymes in organs of female CD rats
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