Smiles-Type Rearrangement ofN-trans-Styrylsulfonyl) andN-(4-Phenyl-1,3-butadienylsulfonyl)thioureas and Isothioureas
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/48/9/48_9_2611/_pdf
Reference4 articles.
1. Synthesis of Arylethylenesulfonamides and Intramolecular Rearrangement ofN-(Arylethylenesulfonyl)thioureas
2. Formation of 5-aryl-5,6-dihydro-4H-1,2,4-thiadiazine 1,1-dioxides and N-trans-styrylamidines by base treatment of N-(trans-styrylsulfonyl) amidines
3. The Synthesis of the New 1,4,2-Dithiazine Ring
4. The Synthesis of the 1,2,4-Thiadiazine-1,1-dioxides
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Efficient Synthesis of N-[4-(4-Chlorophenyl)butyl]-S-(3-piperidinopropyl)isothiourea (OUP-186) and Its Analogues Using 2-Nitrophenylacetyl Isothiocyanate: Application to Novel Histamine H3R Antagonists;Synthesis;2015-03-19
2. Efficient Approaches to S-Alkyl-N-alkylisothioureas: Syntheses of Histamine H3 Antagonist Clobenpropit and Its Analogues;The Journal of Organic Chemistry;2008-02-16
3. ChemInform Abstract: SMILES-TYPE REARRANGEMENT OF N-(TRANS-STYRYLSULFONYL) AND N-(4-PHENYL-1,3-BUTADIENYLSULFONYL)THIOUREAS AND ISOTHIOUREAS;Chemischer Informationsdienst;1975-12-02
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