 | This article is rated Start-class on Wikipedia's content assessment scale. It is of interest to the following WikiProjects: | ||||||||||
| |||||||||||
Untitled edit
From http://www.fmclithium.com/products/products_p.asp?ID=16
Lithium amide is a strong base used primarily in organic synthesis. Typical reactions reported for lithium amide include aldol condensations, alkylations of heterocyclic amines, and formation of cyclopropenes. It is also proven an effective catalyst in transesterification reactions. For leading references, consult 1) J. Am. Chem. Soc. 1894, 65, 517; 2) Handbook in Preparative Inorganic Chemistry, Academic Press, New York, 2nd Ed, 1963, p 463.
http://www.ioc.uni-karlsruhe.de/institut/students/vorlesungen/SS03/MMS/amidebases_by_Hans_Reich.pdf
I added a simple structure of the molecule --PedroDaGr8 22:15, 21 March 2007 (UTC)
http://www3.interscience.wiley.com/journal/26737/home/press/200751press.html
Remark about ternary hydride used for hydrogen storage. Represents an expanded use for lithium amide and lithium borohydride. —Preceding unsigned comment added by Mnpoor (talk • contribs) 22:54, 21 December 2007 (UTC)