Ring-Closing Olefin Metathesis for the Synthesis of 1,8-Diazabicyclo(4. 3.0)non-3-ene-7,9-diones. -The title compounds (II) are of interest due to their potential biological application and as templates in organic synthesis. -(DYATKIN, A.
Ring-closing olefin metathesis for the synthesis of 1,8-diazabicyclo[4.3.0]non-3-ene-7,9-diones
โ Scribed by Alexey B. Dyatkin
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 120 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
A novel method for the efficient synthesis of 1,8-diazabicyclo[4.3.0]non-3-ene-7,9-diones 5 (bicyclic hydantoins) starting from ureas or Z-protected aminoacids has been developed. The key step is a ring-closing metathesis (RCM) reaction of diallyl substituted hydantoins 3 catalyzed by the ruthenium-carbene complex bis(tricyclohexylphosphine)benzilidine ruthenium dichloride (4).
๐ SIMILAR VOLUMES
A Novel Reaction of 1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU) or 1,5-Diazabicyclo[4.3.0]non-5
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