Indole synthesis by controlled carbolithiation of o-aminostyrenes
A Kessler, CM Coleman, P Charoenying…
Index: Journal of Organic Chemistry, , vol. 69, # 23 p. 7836 - 7846
Full Text: HTML
Citation Number: 31
Abstract
... The Journal of ... J. Org. Chem. ... It was demonstrated that by employing diethyl ether as the reaction solvent and maintaining a low temperature, polymerization could be avoided and the generated organolithium product was now available for further organic transformations. ...
Related Articles:
[Bellezza, Francesca; Cipiciani, Antonio; Ruzziconi, Renzo; Spizzichino, Sara Journal of Fluorine Chemistry, 2008 , vol. 129, # 2 p. 97 - 107]
[Journal of the American Chemical Society, , vol. 116, # 26 p. 11723 - 11736]
Indole synthesis by controlled carbolithiation of o-aminostyrenes
[Kessler, Albane; Coleman, Claire M.; Charoenying, Patchanee; O'Shea, Donal F. Journal of Organic Chemistry, 2004 , vol. 69, # 23 p. 7836 - 7846]