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
Synthesis and structure elucidation of a new isoquinolinium inner salt
β Scribed by Ulrich Girreser; Andrzej Czyrski; Tadeusz W. Hermann
- Publisher
- Elsevier Science
- Year
- 2009
- Tongue
- French
- Weight
- 229 KB
- Volume
- 50
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
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 compound. The isolation and structure elucidation of this compound as 2-(2-carboxy-4,5-dimethoxyphenyl)-6,7-dimethoxyisoquinolinium inner salt are reported.
π SIMILAR VOLUMES
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
Synthesis and Structural Elucidation of a New Zooecdysteroid Gerardiasterone. -The synthesis of the title compound (IV), isolated from the mediterranean zoanthid Gerardia savaglia, is achieved via asymmetric dihydroxylation of the E-olefin (III) using equimolar amounts of the hydroxylation system.
The new phase Li 3 Cu 2 SbO 6 , synthesised by solid state reaction at 1000 Β°C, is monoclinic, aβ«,)1(9564.5Ψβ¬ bβ«,)2(2727.8Ψβ¬ cβ«Ψβ¬ 9.7807(3) A s , β«,Β°)2(080.59Ψβ¬ space group C2/c, and has a partially ordered rock salt structure related to the ordered structure of Li 2 TiO 3 by additional cation order