An efficient synthesis of the polar part of sulfamisterin and its analogs
✍ Scribed by Miroslava Martinková; Jozef Gonda; Alena Uhríková; Jana Špaková Raschmanová; Juraj Kuchár
- Book ID
- 113515521
- Publisher
- Elsevier Science
- Year
- 2012
- Tongue
- English
- Weight
- 782 KB
- Volume
- 352
- Category
- Article
- ISSN
- 0008-6215
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
The protected ethidium nucleosides 8-(3%,5%-di-O-benzoyl-2%-deoxy-D-ribofuranosyl)-3-acetamido-5-ethyl-6-phenylphenanthridinium (5), 8-(3%,5%-di-O-acetyl-2%-deoxy-D-ribofuranosyl)-3-acetamido-5-ethyl-6-phenyl-phenanthridinium (6), and the acyclic analog 8-[(3R)-1,3-dihydroxy-4-yl]-acetamido-3-amino-
Benzodiazepines at clinically effective doses often produce side effects like drowsiness, ataxia, or sedation'). Thus, some interest has recently been put to non-diazepine anxiolytic compounds. That resulted in the development of such compounds like buspirone (l), gepirone (2), SM-3997 (3)" or ipsop