A nucleophilic cleavage reaction of 2,2,5,5,8,8-hexamethyl-2,5,8-trisilanona-3,6-diyne, I, with several bases, occurs rapidly at room temperature in both polar and non-polar solvents. An attack occurs exclusively at the central silicon regardless of the steric requirements of the bases (alkyllithium). The major products from the reaction of I with tert-butyllithium followed by hydrolysis were 2,2,5,5,6,6-hexamethyl-2,5-disilahepta-3-yne, II, and 2,2,5,5-tetramethyl-2,5-disilahexa-3-yne, VI.
| Identifer | oai:union.ndltd.org:unt.edu/info:ark/67531/metadc332501 |
| Date | 12 1900 |
| Creators | Jo, Kyo Dong |
| Contributors | Jones, Paul R. |
| Publisher | University of North Texas |
| Source Sets | University of North Texas |
| Language | English |
| Detected Language | English |
| Type | Thesis or Dissertation |
| Format | Text |
| Rights | Public, Jo, Kyo Dong, Copyright, Copyright is held by the author, unless otherwise noted. All rights reserved. |
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