Steric and electronic limitations of the SRN1 reaction between p-nitrobenzylic substrates and tertiary carbanions
BD Jacobs, SJ Kwon, LD Field, RK Norris, D Randles…
Index: Jacobs, Bruce D.; Kwon, Soon-Jae; Field, Leslie D.; Norris, Robert K.; Randles, David; et al. Tetrahedron Letters, 1985 , vol. 26, # 29 p. 3495 - 3498
Full Text: HTML
Citation Number: 9
Abstract
Abstract The S RN 1 reaction between sterically hindered p-nitrobenzylic substrates and tertiary carbanions gives C-alkylated products whose yields depend on the steric bulk of both the benzylic substrate and the carbanion, and on the nature of the groups in the carbanion.
Related Articles:
[Norris,R.K.; Randles,D. Australian Journal of Chemistry, 1976 , vol. 29, p. 2621 - 2629]
[Barker, Steven D.; Norris, Robert K.; Randles, David Australian Journal of Chemistry, 1981 , vol. 34, # 9 p. 1875 - 1878]