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Environmentally Friendly Organic Synthesis Using Bismuth Compounds. Bismuth Trifluoromethanesulfonate-Catalyzed Allylation of Dioxolanes
Australian Journal of Chemistry (2008)
  • Ram S. Mohan, Illinois Wesleyan University
  • Matthew J. Spaffpord
  • James E. Christensen
  • Matthew G. Huddle
  • Joshua R. Lacey
Abstract
A bismuth trifluoromethanesulfonate (triflate)-catalyzed (2.0 mol-%) multicomponent reaction involving the allylation of dioxolanes followed by in situ derivatization with anhydrides to generate highly functionalized esters has been developed under solvent-free conditions. Most reagents used to date for allylation of dioxolanes are highly corrosive and are often required in stoichiometric amounts. In contrast, the use of a relatively non-toxic and non-corrosive bismuth(iii)-based catalyst makes this methodology especially attractive for scale-up.
Keywords
  • Araliphatic ethers,
  • carboxylic acid esters (acyclic compounds),
  • ring opening reactions,
  • multicomponent reactions
Disciplines
Publication Date
2008
Publisher Statement
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Citation Information
Ram S. Mohan, Matthew J. Spaffpord, James E. Christensen, Matthew G. Huddle, et al.. "Environmentally Friendly Organic Synthesis Using Bismuth Compounds. Bismuth Trifluoromethanesulfonate-Catalyzed Allylation of Dioxolanes" Australian Journal of Chemistry Vol. 61 Iss. 6 (2008)
Available at: http://works.bepress.com/ram_mohan/38/