Thermal Rearrangement of 1,3-Thiazolidine Sulfoxides: Thiosulfinate and Thioaldehyde Intermediates. -As an extension of studies on the reactivity and synthetic uses of sulfoxides and sulfenic acids, the thermal rearrangement of title compound (I) is investigated. The formation of the products (II)-
ChemInform Abstract: New Thermal Rearrangement of Vinylogous Ketoketenes and Related Intermediates.
β Scribed by G. A. CARTWRIGHT; R. O. GOULD; H. MCNAB
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 26 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0931-7597
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Thermal Rearrangement of Pyridylnitramines. -In contrast to their N-methyl analogues, which rearrange to form the corresponding methylamino-nitroamines in 74-90% yield, 2-substituted pyridine (I) rearranges into two regioisomers (II) and (III), 4-substituted pyridine (IV) is much less prone to rear
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v