Reaction of 1-α-Cyano-1-deoxynojirimycin with Grignard Compounds—Complete Exchange of the CN— Group
✍ Scribed by Dr. Horst Böshagen; Dr. Walter Geiger; Dr. Bodo Junge
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- English
- Weight
- 252 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0044-8249
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
The reactions of thiobenzamide 8 with diazo compounds proceeded via reactive thiocarbonyl ylides as intermediates, which underwent either a 1,5-dipolar electrocyclization to give the corresponding five membered heterocycles, i.e., 4-amino-4,5-dihydro-1,3-thiazole derivatives (i.e., 10a, 10b, 10c, ci
The active ketenylidene-(2a) or thioketenylidenetriphenylphosphoranes (2b) react with 2-benzylidene-1,3-indandione (1), 5-benzylidenebarbituric acid (11), and 4-benzylidene-1,2-diphenyl-3,5-pyrazolidinedione (16) to give the corresponding pyranones and thioxopyranones (3a,b, 12a,b) and (17a,b), resp
The addition of a catalytic amount of Cp2TiC12 to an ether solution of propylmagnesium bromide and 1,3-dienes brings about an