Fulven-Dimere und -Trimere. Hinweis auf eine [6 + 4]-Cycloaddition von 6,6-Dimethylfulven
In contrast to earlier assumptions, thermal reaction of simple fulvenes 1a, b, c at 20°C gives Diels-Alder-dimers 2a, b, c in a relatively high yield. Whereas the dimers 2b and 2c equilibrate easily with the corresponding fulvenes at 60 °C, heating of the fulvene-dimer 2a produces an equilibrium 2a...
Saved in:
| Main Authors: | Beat Uebersax, Markus Neuenschwander |
|---|---|
| Format: | Article |
| Language: | deu |
| Published: |
Swiss Chemical Society
1981-10-01
|
| Series: | CHIMIA |
| Online Access: | https://www.chimia.ch/chimia/article/view/9536 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
The Ozonolysis of α-Terpineol - Unusual Formation of a 6,6-Dimethylfulvene Epoxide
by: Alan F. Thomas, et al.
Published: (1985-08-01) -
Über ein rotes C8-Fulven
by: H. Schaltegger, et al.
Published: (1962-07-01) -
Synthese und Luftvernetzung von Dimethylfulven-Copolymerisaten
by: Ulrich Schädeli, et al.
Published: (1986-08-01) -
Photochemical Cycloadditions to 5,6-Dihydro-4-pyridones
by: Philippe Guerry, et al.
Published: (1987-10-01) -
Finishing of polyamide fabric 6 and polyamide 6.6 fabric with some boron compounds
by: Nikodijević Milena
Published: (2025-01-01)