Elimination of Substituted Fluoren-9-ylmethyl Benzenesulfonates: Hammett Substituent Effects at a Mechanistic Borderline

…, RA More O'Ferrall, DG Murphy

Index: Larkin, Finbar G.; More O'Ferrall, Rory A.; Murphy, Donal G. Collection of Czechoslovak Chemical Communications, 1999 , vol. 64, # 11 p. 1833 - 1848

Full Text: HTML

Citation Number: 10

Abstract

Abstract Rates of elimination of fourteen substituted fluoren-9-ylmethyl benzenesulfonates have been measured in methanolic sodium methoxide and 90% aqueous ethanolic solutions of triethylamine, trimethylamine and 4-methyl morpholine. For the sodium methoxide, a linear Hammett plot with ρ= 0.74, consistent with reaction by an E2 mechanism, is observed. For the amine bases the Hammett plots are curved, suggesting a ...

Related Articles:

Direct conversion of thiols to sulfonyl chlorides and sulfonamides

[Bahrami, Kiumars; Khodaei, Mohammad M.; Soheilizad, Mehdi Journal of Organic Chemistry, 2009 , vol. 74, # 24 p. 9287 - 9291]

Synthesis of Sulfonyl Chlorides and Sulfonic Acids in SDS Micelles

[Bahrami, Kiumars; Khodaei, Mohammad M.; Abbasi, Jamshid Synthesis, 2012 , vol. 2012, # 2 p. 316 - 322]

More Articles...