Novel Intramolecular Cyclization Reaction Involving a Thionitroso Group: Formation of a 3,3a-Dihydro-2,1-benzisothiazole from an o-Alkylthionitrosoarene
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/27/10/27_10_981/_pdf
Reference7 articles.
1. The Chemistry of Thionitroso Compounds
2. Spectroscopic detection and reactions of a thionitroso compound
3. Synthesis and structure of a novel molecular bowl with an all-carbon and acyclic framework
4. Synthesis, Structure, and Reactions of a Sulfenic Acid Bearing a Novel Bowl-Type Substituent: The First Synthesis of a Stable Sulfenic Acid by Direct Oxidation of a Thiol
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1. Sulfur monochloride in organic synthesis;Russian Chemical Reviews;2014-03-28
2. ChemInform Abstract: Novel Intramolecular Cyclization Reaction Involving a Thionitroso Group: Formation of a 3,3a-Dihydro-2,1-benzisothiazole from an o-Alkylthionitrosoarene.;ChemInform;2010-06-17
3. Syntheses of shuttlecock- and bowl-equipped phenylazopyridines and photomodulation of their coordination ability to Zn-porphyrin;Tetrahedron Letters;2009-05
4. Isothiazoles;Comprehensive Heterocyclic Chemistry III;2008
5. Nanoscale Molecular Cavities for Stabilization of Highly Reactive Species;Journal of Synthetic Organic Chemistry, Japan;2005
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