Synthesis of novel N-aroyl- and N-arylsulfonylisothiazole-2-imines by cyclization of thiocyanatovinylaldehyde hydrazones
✍ Scribed by Bärbel Schulze; Kerstin Mütze; Dagmar Selke; Rhett Kempe
- Book ID
- 104224990
- Publisher
- Elsevier Science
- Year
- 1993
- Tongue
- French
- Weight
- 242 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
Tbe synthesis olN-sroyl-and N-arylsulfonyli~~irzole-2-lmines 7e-f as well as the correspolldiw acceptowtbstltuted~2aminoisothiazolium salts &-f by cyclocondcnsation of tbiocyanatovinylaldebyde hydrazones (r-f is npti. The alternative cyckation route to 1,2,34hiadiazines is not observed.
📜 SIMILAR VOLUMES
The acid-catalyzed cyclization of N- [2-(cyclohex-1-octahydroisoquinoline formed was accompanied by minor concentrations of one, two, or three isomeric octa-enyl)ethyl]-N-styrylformamides 1-5 gave access to 1-benzyl-2-formyloctahydroisoquinolines 6-10. The reactions were hydroisoquinolines. 1-Benzyl