Ring closure in 1,2-divinylcyclohexanes and isomerization to 3-methyl-3a,4,5,6,7,7a-hexahydro-1h-indenes catalyzed by titanocene hydride derivatives
✍ Scribed by K. Mach; P. Sedmera; L. Petrusová; H. Antropiusová; V. Hanuš; F. Tureček
- Publisher
- Elsevier Science
- Year
- 1982
- Tongue
- French
- Weight
- 231 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Titanocene hydride derivatives induce the cyclization of 1,2-divinylcyclohexanes to trans-and cis-1-methylene-octahydro-lH-indene and their isomerization to transand cis-3-methyl-3a,4,5,6,7,7a-hexahydro-lH-indene.
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The title compound, C 10 H 14 N 4 O 3 S, is the first example of the fused tricyclic octahydro-1-thia-2,3a,8a-triazacyclopenta[a]indene ring system. The S-containing heterocycle adopts a typical envelope conformation, fused at the 2,3-positions to a 2,3a,4,5,6,7-hexahydroindazol-3-one unit.