**Facile synthesis of derivatives of 2,4‐diphenyl‐3‐azabicyclo[3.3.1]nonane and 7,9‐diphenyl‐8‐azabicyclo[4.3.1]decane** The facile synthesis of hydantoins, cyanhydrins and aminonitriles derived from 2,4‐diphenyl‐3‐azabicyclo[3.3.1]nonanone and 7,9‐diphenyl‐8‐azabicyclo[4.3.1]decanone is described.
✦ LIBER ✦
Synthèse de spirohydantoines dérivées du diphényl-2,4-aza-3-bicyclo-[3.3.1]nonane et du diphényl-7,9-aza-8-bicyclo[4.3.1]decane par réaction de Bucherer dans la N,N-diméthylformamide: Influence de la température et cours stéréochimique. Communication préliminaire
✍ Scribed by Ernesto Martínez; Carmen del Campo; Gregorio G. Trigo
- Publisher
- John Wiley and Sons
- Year
- 1983
- Tongue
- German
- Weight
- 212 KB
- Volume
- 66
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Synthesis of Spyrohydantoines Derivatives of 2,4‐Diphenyl‐3‐azabicyclo[3.3.1]nonane and 7,9‐Diphenyl‐8‐azabicyclo[4.3.1]decane via Bucherer Reaction in N,N‐Dimethylformamide: Influence of the Temperature and Stereochemical Path
The unreactives ketones related to 2,4‐diphenyl‐3‐azabicyclo [3.3.1]nonan‐9‐one to the Bucherer reaction in usuals conditions show excellent reactivity in DMF. as unique solvant. The stereochemical paths of these reactions and the synthetic utility of the temperature modification are described.
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✍
Carmen Del Campo; Ernesto Martinez; Gregorio G. Trigo
📂
Article
📅
1984
🏛
John Wiley and Sons
🌐
German
⚖ 335 KB
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