Rearrangement of Aryl- and Benzylthiopyridinium Imides with Participation of a Methyl Substituent
Author:
Affiliation:
1. Chemical Research Center, Hungarian Academy of Sciences, H-1025 Budapest, Pusztaszeri út 59-67, Hungary
2. Institute of Chemistry and Biochemistry, AS CR, Flemingovo nám. 2, 16610 Prague, Czech Republic
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo201645t
Reference23 articles.
1. Synthesis of new stable arylthiopyridinium N-arylimide zwitterions. Part 20: Fused azolium salts
2. Unexpected Ring Transformation to Pyrrolo[3.2-b]pyridine Derivatives. Fused Azolium Salts. 22
3. New Facile Tandem Route to Oxo- and Thioxo[1,2,4]triazolo[1,5-a]pyridinium Salts
4. Formation of new pyridyl substituted enamines. Observation of a diaza-Cope rearrangement
5. Synthesis and nitrogen elimination of 3-aryltetrazolo(1, 5-a)pyridinium salts and its angular benzenologues
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