Imidothiocarbonates. V. Preparations and Properties of Novel Azomethine Ylides and Thiocarbonyl Ylides from Sulfur-contained Heterocycles
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/45/6/45_6_1797/_pdf
Reference9 articles.
1. Iminodithiocarbonates. III. Reactions with Some Electrophiles and the Structural Effect on Nucleophilic Reactivities and Basicities
2. 1,3-Dipolar Cycloadditions. Past and Future
3. 2-Substituted Imino-1,3-dithiolanes. Their Thermal Ring-isomerizations and Reactions with Epoxides
4. Reactions of Various Thione-compounds with Epoxides. A New Method for the Transformation of the C=S Bond into the C=O
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2. 2-halogen-substituted pyridinium-N-phenacylides and their cycloiminium and acyclic analogs: 1. Synthesis of the parent salts, their betaine-ylides, and oxazolium analogs;Review Journal of Chemistry;2011-04
3. Synthesis of Five-Membered Sulfur-Heterocycles via 1,5-Dipolar Electrocyclization of Thiocarbonyl Ylides and Related Processes;Current Organic Chemistry;2011-03-01
4. Reactions of 1,5-π-cyclization of gem-difluoro-substituted azomethine ylides involving an aromatic ring;Russian Journal of Organic Chemistry;2006-05
5. 1,5-Dipolare Elektrocyclisierung von Acyl-substituierten ‘Thiocarbonyl-yliden’ zu 1,3-Oxathiolen;Helvetica Chimica Acta;1996-05-08
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