Evaluation of lithium amide base formation at low temperature via carbon-13 NMR spectroscopy
KF Podraza, RL Bassfield
Index: Podraza, Kenneth F.; Bassfield, Ronald L. Journal of Organic Chemistry, 1988 , vol. 53, # 11 p. 2643 - 2644
Full Text: HTML
Citation Number: 20
Abstract
0022-3263/88/1953-2643 $01.50/0 tetramethylpiperidide (LTMP) to name a few. The usefulness of lithium amide bases in carbanion formation is well established., As a result of their popularity, the preparation of each respective base has been accomplished by a wide variety of experimental conditions. For instance, LDA has been prepared by the addition of n- butyllithium in hexane to a solution of diisopropylamine in tetrahydrofuran (THF) at 0" C ...
Related Articles:
[Lappert, Michael F.; Slade, Martin J.; Singh, Anirudh; Atwood, Jerry L.; Rogers, Robin D.; Shakir, Riz Journal of the American Chemical Society, 1983 , vol. 105, # 2 p. 302 - 304]
Acidity measurements on pyridines in tetrahydrofuran using lithiated silylamines
[Fraser, Robert R.; Mansour, Tarek S.; Savard, Sylvain Journal of Organic Chemistry, 1985 , vol. 50, # 17 p. 3232 - 3234]
Lithium dialkylamides. 13C parameters and slow proton transfer
[Fraser, Robert R.; Baignee, Alison; Bresse, Monique; Hata, Kazumi Tetrahedron Letters, 1982 , vol. 23, # 41 p. 4195 - 4198]