Preparation, Structure, and Reactivity of 1,3,4-Triphenyl-4,5-dihydro-1H-1,2,4-triazol-5-ylidene, a New Stable Carbene
β Scribed by Prof. Dr. Dieter Enders; Dipl.-Chem. Klaus Breuer; Dr. Gerhard Raabe; Dr. Jan Runsink; Dr. J. Henrique Teles; Dr. Johann-Peter Melder; Dr. Klaus Ebel; Dr. Stefan Brode
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 386 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0044-8249
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
5(4H)-ones / 2-Chloro-N-cyanomethyl-N-methylnicotinamide / Aromatic nucleophilic substitution A new synthesis of pyrido[3,2-f][1,4]thiazepine derivatives 3 starting with 2-chloronicotinic acid (1), methylaminoacetonitrile hydrochloride and carbon disulfide is described. As proved by a crystal struct
and 3-aminopyrazole and 3-amino-1,2,4-triazole provide convenient access to biologically relevant 3H-imidazo[1,2-b]pyrazoles and a 5H-imidazo[2,1-c][1,2,4]triazole.