## Abstract 1,3,4(2__H__)‐Isochinolintrione **1** reagieren mit Ethanol, Aminen (auch mit 6‐Aminopenicillansäure) oder Hydrazin unter Bildung von Estern **3**, Amiden **5, 8** bzw. Hydraziden **9, 10** der 1‐Hydroxy‐3‐oxoisoindolin‐1‐carbonsäure.
Wertschöpfung aus einem Abfallstoff: Methylierung von Aminen mit CO 2 und H 2
✍ Scribed by Tlili, Anis; Frogneux, Xavier; Blondiaux, Enguerrand; Cantat, Thibault
- Book ID
- 123619927
- Publisher
- John Wiley and Sons
- Year
- 2014
- Tongue
- English
- Weight
- 465 KB
- Volume
- 126
- Category
- Article
- ISSN
- 0044-8249
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Reaction of alkenediazonium salts 1 with ,,mines" 2 (primary amines, hydrazines, hydroxylamine ethers) leads to 2-diazoimines 4, lH-l,2,3-triazoles 6, and imido esters 8 and 9, respectively, depending on the substituents R. Condensation of l-amino-lH-l,2,3-triazole 6Caa with acetone yields hydrazone
Boron‐Trifluoride‐Catalyzed Reactions of 3‐Amino‐2__H__‐azirines with Amino‐acid Esters and Amines After activation by protonation or complexation with BF~3~, 3‐amino‐2__H__‐azirines 1 react with the amino group of α‐amino‐acid esters 3 to give 3,6‐dihydro‐5‐aminopyrazin‐2(1__H__)‐ones 4 by ring en