## Abstract The products of the addition of nucleophiles (alcohols, amines) to the cyano group of 5โ(cyanoimino)thiadiazolines 1 undergo a BoultonโKatritzky rearrangement. The thiadiazoles 4 are formed by subsequent nitrile elimination. In the case of bicyclic thiadiazoloazepine 5 an equilibrium mi
โฆ LIBER โฆ
Synthesis of Isoxazoline Derivatives through Boulton-Katritzky Rearrangement of 1,2,4-Oxadiazoles
โ Scribed by Palumbo Piccionello, Antonio; Guarcello, Annalisa; Pace, Andrea; Buscemi, Silvestre
- Book ID
- 120042580
- Publisher
- John Wiley and Sons
- Year
- 2013
- Tongue
- English
- Weight
- 440 KB
- Volume
- 2013
- Category
- Article
- ISSN
- 1434-193X
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