Lithium Trifluoromethanesulfonimide in Acetone Or Diethyl-ether As a Safe Alternative To Lithium Perchlorate in Diethyl-ether for Effecting Diels-alder Reactions - Unexpected Influence of the Counterion On Exo/endo Selectivity

Handy, ST.;Grieco, PA.;Mineur, C.;Ghosez, Léon
(1995) Synlett : accounts and rapid communications in synthetic organic chemistry — n° 5, p. 565-567 (1995)

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  • Handy, ST.
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  • Grieco, PA.
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  • Mineur, C.
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  • Ghosez, LéonUCLouvain
    Author
Abstract
Concentrated solutions of lithium trifluoromethanesulfonimide in either acetone or diethyl ether constitute convenient and safe alternatives to lithium perchlorate in diethyl ether for promoting and accelerating [4+2] cycloaddition reactions.
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Handy, ST., Grieco, PA., Mineur, C., & Ghosez, L. (1995). Lithium Trifluoromethanesulfonimide in Acetone Or Diethyl-ether As a Safe Alternative To Lithium Perchlorate in Diethyl-ether for Effecting Diels-alder Reactions - Unexpected Influence of the Counterion On Exo/endo Selectivity. Synlett : accounts and rapid communications in synthetic organic chemistry, 5, 565-567. https://doi.org/10.1055/s-1995-5289 (Original work published 1995)