Ein 1,5-Diazabicyclo[3.3.0]octa-2,7-dien aus Acetylendicarbonsäure-dimethylester und einem 3,5-Dihydro-4H-1,2,3-triazol-4-on
✍ Scribed by Quast, Helmut ;Meichsner, Georg ;Regnat, Dieter ;Banert, Klaus ;Peters, Eva-Maria ;Peters, Karl ;von Schnering, Hans Georg
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 311 KB
- Volume
- 1990
- Category
- Article
- ISSN
- 0947-3440
No coin nor oath required. For personal study only.
✦ Synopsis
A 1,5‐Diazabicyclo[3.3.0]octa‐2,7‐diene is Formed from Dimethyl Acetylenedicarboxylate and a 3,5‐Dihydro‐4__H__‐1,2,3‐triazol‐4‐one
The 3,5,5‐trialkyl‐3,5‐dihydro‐4__H__‐1,2,3‐triazol‐4‐one 1 and dimethyl acetylenedicarboxylate (2) react slowly at 50°C in a 1 : 1 ratio to afford a 40% yield of a deep red crystalline product C~18~H~24~N~2~O~8~. ^1^H‐, ^13^C‐ and ^15^N‐NMR spectra and an X‐ray diffraction analysis prove the structure 6 for the red product.
📜 SIMILAR VOLUMES
Aziridinone / u-Lactam 1 Decarbonylation Photolysis of 3-Methyl-5.5-dipheny1-3,5-dihydro-4H-1,2,3-tria~ol-4-0ne~'~ Irradiation (h 2 280 nm) of a degassed solution in deuterated benzene of the dihydro-1,2,3-triazolone 5 yields the dihydroin-dolone 7, the imine 9, and its photoreduction product 10, be
## Abstract Durch Umsetzung der 5‐Aryloxazole **2a**–**e** sowie der substituierten Vertreter **8a**–**c** und **10** mit 4‐Phenyl‐4__H__‐1,2,4‐triazol‐3,5‐dion (**3**) lassen sich die neuen 7‐Aroyl‐1__H__,7__H____s__‐triazolo[1,2‐__a__]‐__s__‐ triazol‐1,3(2__H__)‐dione **5a**–**e**, **9a**–**c** u