Synthesis and Structure Elucidation of a New Potent Sandalwood-Oil Substitute
✍ Scribed by Jerzy A. Bajgrowicz; Iris Frank; Georg Fráter; Michael Hennig
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- German
- Weight
- 685 KB
- Volume
- 81
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Spirocephams 4 and S have been obtained from aldehyde 1 and hydroxylamine or hydrazine, as single diastereoisomers. Structures of these compounds have been elucidated by NME experiments and FIND0 calculations. In the course of a prograssne to design cephems modified at the 3 position, we condensed
Papaverine is a drug that can be easily oxidized to papaverinol, papaveraldine and to recently discovered 2,3,9,10-tetramethoxy-12-oxo-12H-indolo[2,1-a]isoquinolinium chloride. In a strong alkaline medium the spectroscopic properties of this latter compound are modified indicating formation of a new
Synthesis and Structure Elucidation of New Thiazolotriazepines. -New title compounds, which are of biological interest, can be prepared by reaction of triazepinethiones like (II) with 2-haloketones or condensation of chalcones with iminothiazolines. Their structures are determined by comprehensive o