Synthesis of functionalized 1,5-cyclooctadienes by LICKOR metalation
Revell, J. D. and Ganesan, A. (2002) Synthesis of functionalized 1,5-cyclooctadienes by LICKOR metalation. Journal of Organic Chemistry, 67, (17), 6250-6252. (doi: 10.1021/jo025715u).
Download
Full text not available from this repository.
Original Publication URL: http://pubs3.acs.org/acs/journals/doilookup?in_doi...
Description/Abstract
1,5-Cyclooctadiene was lithiated under LICKOR superbase conditions followed by reaction with alkyl halides or ethylene oxide to yield 3-substituted 1,5-cyclooetadienes in high yield and purity. This procedure is suitable for preparation of 1,5-cyclooctadienes carrying pendant functional groups for immobilization on solid-phase resins.
| Item Type: | Article |
|---|---|
| Related URLs: | |
| Keywords: | 9-borabicyclononane 9-bbn, organic-synthesis, superbases, route |
| Subjects: | Q Science Q Science > QD Chemistry |
| Divisions: | University Structure - Pre August 2011 > School of Chemistry |
| Item ID: | 19843 |
| Date Deposited: | 20 Feb 2006 |
| Last Modified: | 01 Jun 2011 06:14 |
| Contributors: | Revell, J. D. (Author) Ganesan, A. (Author) |
| Date: | 23 August 2002 |
| Status: | Published |
| URI: | http://eprints.soton.ac.uk/id/eprint/19843 |
Actions (login required)
 |
View Item |
