Highly Stereoselective Synthesis, Structure, and Application of ( E ) - 9-[2-(Silyl)ethenyl]-9 H -carbazoles
✍ Scribed by Marciniec, Bogdan; Majchrzak, Mariusz; Prukała, Wiesław; Kubicki, Maciej; Chadyniak, Dariusz
- Book ID
- 121881290
- Publisher
- American Chemical Society
- Year
- 2005
- Tongue
- English
- Weight
- 157 KB
- Volume
- 70
- Category
- Article
- ISSN
- 0022-3263
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📜 SIMILAR VOLUMES
Aryl-substituted tricarbonyl(rl4-cyclohexa -1,3-diene)iron complexes are oxidatively cyclized in protic medium in the air to tricarbonyliron-complexed 4a,9a-dihydro-9H-carbazoles. The method is applied to the total synthesis of mukonine and mukonidine.
Transition-Metal Complexes in Organic Synthesis. Part 36. Cyclization of Tricarbonyliron Complexes by Oxygen to 4a,9a-Dihydro-9Hcarbazoles: Application to the Synthesis of Mukonine, Mukonidine, and Pyrido(3,2,1-jk)carbazoles. -A novel method for the cyclization of aryl-substituted iron complexes su
## Abstract Three new compounds based on carbazole planar skeleton were synthesised. Among them there is a new ligand and a potential DNA intercalator which contains a benzothiazolium moiety connected to the carbazole ring by a vinyl bridge. The absorption and emission spectral properties of this n
## Abstract The methanesulfonic acid catalyzed reaction of 1‐(4‐chloro‐ and 2,4‐dichlorophenyl)‐2‐(1‐methyl‐2‐imida‐zolyl)ethanones 1a and 1b with glycerol produced __cis__‐ and __trans__‐{2‐haloaryl‐2‐[(1‐methyl‐2‐imidazolyl)methyl]‐4‐hydroxymethyl}‐1,3‐dioxolanes 2a and 2b with a 2:1 __cis/trans_