- PII
- 10.31857/S0044460X23050013-1
- DOI
- 10.31857/S0044460X23050013
- Publication type
- Article
- Status
- Published
- Authors
- Volume/ Edition
- Volume 93 / Issue number 5
- Pages
- 659-663
- Abstract
- The sulfonamide with a benzothiazine moiety was synthesized by a Diels-Alder reaction of thionylaniline with dicyclopentadiene. The prepared adduct was oxidized to the appropriate sulfonamide with a benzothiazine moiety. The molecular and crystal structure of the sulfonamide obtained was determined by the single crystal X-ray diffraction analysis. A higher reactivity of the the olefin function of the norbornene fragment was found; and the formation of two structural isomers was revealed.
- Keywords
- сульфонамиды реакция Дильса-Альдера сокристаллизация
- Date of publication
- 17.09.2025
- Year of publication
- 2025
- Number of purchasers
- 0
- Views
- 15
References
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