## Abstract __X__‐ray structure analysis of the title compound (I) is reported. The results are interpreted to predict formation of __anti__‐tricyclo[4.4.0^1,6^.0^7,12^]‐1,4,7,10‐tetraethoxycarbonyl‐3,6,9,12‐tetrahydroxy‐dodeca‐3,9‐diene on UV.‐irradiation of solid (I).
Chemistry of Succinylsuccinic Acid Derivatives. Part I. On the photodimerization of diethyl succinylsuccinate
✍ Scribed by Joel Sinnreich; Hans Batzer
- Publisher
- John Wiley and Sons
- Year
- 1973
- Tongue
- German
- Weight
- 331 KB
- Volume
- 56
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
Topochemically controlled photochemical dimerization of diethyl succinylsuccinate in the solid is reported. The structure evaluation by elemental and spectroscopic analysis of the product is given. The participation of chelated enols in photochemical cycloadditions in the crystalline solid state is here demonstrated for the first time.
📜 SIMILAR VOLUMES
## Abstract __X__‐ray structure analysis of the title compound (II) is reported. Diffractometer data and the Faltmolekül method were used. Refinement converged at R 0.044. The molecule assumes the __syn,syn__‐conformation in the crystal.
## Abstract The Preparation of 2 new tetrasubstituted cyclohexane isomers by hydrogenation of diethyl succinyl succinate is reported. A route for their formation is postulated.
## Abstract The unique stabilization of the ester link in dialkyl succinyl succinates is explained and a facile route to known as well as to hitherto inaccessible succinyl succinates is suggested. New representatives of this series are described.
Acidic hydrolysis and cyclization were studied in vincoside glycosides ('natural' series) and their dihydro derivatives ('dihydro' series) in which either one or both N atoms were free or blocked by an alkyl group. For interpretation of the results, a graph was constructed in which 25 points (actual