Attempted reformatskii reaction of benzonitrile, 1,4-diketo-3,6-diphenylpyrrolo[3,4-C]pyrrole. A lactam analogue of pentalene.
β Scribed by Donald G. Farnum; Goverdhan Mehta; George G.I. Moore; Frederick P. Siegal
- Book ID
- 104244317
- Publisher
- Elsevier Science
- Year
- 1974
- Tongue
- French
- Weight
- 185 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
Some time ago we became interested in the synthesis of derivatives of Z-azetlnone (1). a lactam analogue of the "antiaromatic" hydrocarbon, cyclobutadiene.
It seemed possible that a modification of the Reformatskii reaction, already used for the synthesis of Z-azetidinones, or g-lactams,
1 might yield Z-azetinones as well , as shown in equations ( ) and ( ).
π SIMILAR VOLUMES
## Abstract **Summary:** The photophysical properties of dendrimers with 1,4βdioxoβ3,6βdiphenylpyrrolo[3,4βc]pyrrole, also known as DPP, as a core were studied. DPP itself has a high quantum yield of fluorescence, as well as a high molar decadic absorption coefficient, __Ξ΅__ (__Ξ΅__β=β33β000 LβΒ·βmol