Ring expansion by sulphur migration: Synthesis of 2-alkylidene-1,4-benzodithians and 1,4-benzodithiins
β Scribed by Philip Blatcher; Stuart Warren; Smollie Ncube; Andrew Pelter; Keith Smith
- Publisher
- Elsevier Science
- Year
- 1978
- Tongue
- French
- Weight
- 183 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Reaction of 2-(l-hydroxyalkyll-1,3-bensodithioles (1) with thionyl chloridetriethylamine gives high yields of 2-alkylidene-3-substituted benzodithians, and 2,3-substituted benzodithiins on treatment with acid.
π SIMILAR VOLUMES
Synthesis of 2-Alkylidene-3,3-dialkyl-1,4-dithianes and Their Oxathiane Analogues by 1,2-Sulfur Migration. -Base-promoted mesylation of tertiary alcohols such as (I) and (III) derived from dithianes or oxathianes results in rearrangement by sulfur migration to yield the 1,4-dithianes (II) and their
## Abstract A straight forward synthesis of the 1,4,2βbenzodithiazine system bearing an ester functionality as potential inducers of systemic acquired resistance in plants was developed utilizing the ring expansion reaction of 1,3βbenzodithioles. The structure of the isomers obtained was establishe