Synthesis of 6,6-Dimethyl-2-Cyclopentadienylethylbicyclo[3.1.1] Hept-2-Ene and of 6,6-Dimethyl-2-Indenylethylbicyclo[3.1.1] Hept-2-Ene.

Authors

  • gloria obuzor

ligand, metallocene, cyclopentadienyl, indenyl, organ metallic, n-buthyllithium

Abstract

The new compounds 6,6-dimethyl-2-cyclopentadienylethylbicyclo[3.1.1] hept-2-ene (4) and 6,6-dimethyl-2-indenylethylbicyclo[3.1.1] hept-2-ene (5) were synthesized in 82% and 60% yield respectively using 6,6-dimethyl-2-p-toluenesulphonyloxomethylbicyclo[3.1.1] hept-2-ene (2). However, compounds -(4) and (5) were obtained in 71% and 81% yield respectively using 6,6-dimethyl-2-sulphonyloxomethylbicyclo[3.1.1] hept-2-ene (3). All compounds were characterized by NMR, Infra-red, Micro Analysis and Mass Spectroscopy.

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Synthesis of 6,6-Dimethyl-2-Cyclopentadienylethylbicyclo[3.1.1] Hept-2-Ene and of 6,6-Dimethyl-2-Indenylethylbicyclo[3.1.1] Hept-2-Ene. (2013). Global Journal of Science Frontier Research, 13(B5), 9-12. https://www.journalofscience.org/index.php/GJSFR/article/view/903

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Synthesis of 6,6-Dimethyl-2-Cyclopentadienylethylbicyclo[3.1.1] Hept-2-Ene and of 6,6-Dimethyl-2-Indenylethylbicyclo[3.1.1] Hept-2-Ene.

Published

2013-08-03

How to Cite

Synthesis of 6,6-Dimethyl-2-Cyclopentadienylethylbicyclo[3.1.1] Hept-2-Ene and of 6,6-Dimethyl-2-Indenylethylbicyclo[3.1.1] Hept-2-Ene. (2013). Global Journal of Science Frontier Research, 13(B5), 9-12. https://www.journalofscience.org/index.php/GJSFR/article/view/903