## Abstract The reaction of 2‐naphthol‐1‐sulfonic acid with diazonium salts was investigated in the pH range 10 to 15. The structures postulated for the reaction products by __Rowe et al.__ [3] and by __Koller__ [4] were proved by instrumental analysis. In alkaline solutions, instead of the usual d
Zur Stereochemie der Ringöffnung von trans-1,2-Diphenylcyclopropanen mit Quecksilber(II)salzen
✍ Scribed by Dr. S. G. Bandaev; Prof. Dr. Yu. S. Šabarov; A. Hantschmann; Prof. Dr. M. Weissenfels
- Publisher
- John Wiley and Sons
- Year
- 1980
- Tongue
- English
- Weight
- 333 KB
- Volume
- 322
- Category
- Article
- ISSN
- 1615-4150
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✦ Synopsis
Stereochemistry of Ring Opening of trans‐1,2‐Diphenylcyclopropanes by Mercury(II) salts
Reaction of trans‐1,2‐diphenylcyclopropanes 1 and 2 with mercuric salts yields diastereomeric 1,2‐diphenylpropanole derivatives. The ratio of erythro and threo diastereomers depends on the nature of substituents and solvent properties.
A mechanism is proposed to explain the different product ratios.
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