## 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 “Full Text” option. The original article is trackable v
Synthesis of 1,4,2-benzodithiazine carboxylates via ring expansion reaction of 1,3-benzodithioles
✍ Scribed by Peter Stanetty; Gregor Hattinger; Marko D. Mihovilovic; Kurt Mereiter
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2000
- Tongue
- English
- Weight
- 317 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
Abstract
A straight forward synthesis of the 1,4,2‐benzodithiazine system bearing an ester functionality as potential inducers of systemic acquired resistance in plants was developed utilizing the ring expansion reaction of 1,3‐benzodithioles. The structure of the isomers obtained was established using x‐ray diffraction. The reactivity of the products towards activated alkynes and ring contraction reactions in the presence of base is discussed.
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## 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, please click on HTML or PDF.
## Abstract magnified image A new simple synthetic approach to 2,4‐difuryl‐4__H__‐3,1‐benzothiazines from 2‐isothiocyanoaryldifuryl‐methanes in the presence of acidic catalyst is described. This rearrangement is a new example of furan ring migration reaction resulting from intramolecular attack wi