Professor Philip Dyer p.w.dyer@durham.ac.uk
Professor
Sterically-controlled regioselective para-substitutions of aniline
Dyer, P.W.; Fawcett, J.; Griffith, G.A.; Hanton, M.J.; Olivier, C.; Patterson, A.R.; Suhard, S.
Authors
J. Fawcett
G.A. Griffith
M.J. Hanton
C. Olivier
A.R. Patterson
S. Suhard
Abstract
Introduction of sterically demanding 1-isopropyl-2-methyl-propyl or triisopropylsilyl groups at the nitrogen of aniline allows high-yielding regioselective para-substitution to be achieved using a lithiation/substitution sequence.
Citation
Dyer, P., Fawcett, J., Griffith, G., Hanton, M., Olivier, C., Patterson, A., & Suhard, S. (2005). Sterically-controlled regioselective para-substitutions of aniline. Chemical Communications, 3835-3837. https://doi.org/10.1039/b506824j
Journal Article Type | Article |
---|---|
Publication Date | Jun 1, 2005 |
Deposit Date | May 10, 2007 |
Journal | Chemical Communications |
Print ISSN | 1359-7345 |
Electronic ISSN | 1364-548X |
Publisher | Royal Society of Chemistry |
Peer Reviewed | Peer Reviewed |
Issue | 30 |
Pages | 3835-3837 |
DOI | https://doi.org/10.1039/b506824j |
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