We found that the ring-opening fluorination of terminal epoxidesusing TBABF-KHF2 proceeds with high selectivity throughthe SN2 mechanism. As TBABF-KHF2 iseasily obtainable, is stable, and can be used in glassware, it canbe a useful reagent for 1-fluoro-2-alkanol synthesis from the terminalepoxides
The use of trialkylorganozincates and tetraalkylaluminates allows regioselective SN2 nucleophilic op...
A convenient and metal/catalyst-free approach for the reversal of regioselectivity in nucleophilic f...
A variety of epoxides undergo rapid ring opening with ammonium thiocyanate in the presence of 10 mol...
The utility of fluorine in medicinal and manufacturing chemistry is undisputed. Despite its usefulne...
The regioselective opening of epoxides with organotin oxides 1 and 2, in presence of halogenated alc...
Tetrabutylammonium dihydrogentrifluoride, Bu(4)N(+)H(2)F(3)(-), was found to be a very efficient cat...
Tetrabutylammonium fluoride (1) catalyses under mild conditions the opening of epoxides 2a-k with th...
Treatment of a range of 2,3- and 3,4-epoxy amines with HBF(4)·OEt(2) at room temperature results in ...
This thesis describes investigations into the utility of boron fluorides and tetrafluoroborates as s...
A novel selective and substrate-dependent synthetic protocol has been developed towards the synthesi...
Organolithium reagents effect a regioselective SN2 nucleophilic cleavage of a,ß-ethylenic epoxides o...
Herein, we report a study on the reactivity of three 1,3-diarylimidazolium-based fluoride reagents, ...
MPV type reaction In the previous note,1 we reported that Al-methanesulfonyl-diisobutylalane (DIBAO3...
International audienceThe activation of SF6, a potent greenhouse gas, under metal-free and visible l...
The development of organofluorine chemistry has revolutionised the way many agrochemical and pharmac...
The use of trialkylorganozincates and tetraalkylaluminates allows regioselective SN2 nucleophilic op...
A convenient and metal/catalyst-free approach for the reversal of regioselectivity in nucleophilic f...
A variety of epoxides undergo rapid ring opening with ammonium thiocyanate in the presence of 10 mol...
The utility of fluorine in medicinal and manufacturing chemistry is undisputed. Despite its usefulne...
The regioselective opening of epoxides with organotin oxides 1 and 2, in presence of halogenated alc...
Tetrabutylammonium dihydrogentrifluoride, Bu(4)N(+)H(2)F(3)(-), was found to be a very efficient cat...
Tetrabutylammonium fluoride (1) catalyses under mild conditions the opening of epoxides 2a-k with th...
Treatment of a range of 2,3- and 3,4-epoxy amines with HBF(4)·OEt(2) at room temperature results in ...
This thesis describes investigations into the utility of boron fluorides and tetrafluoroborates as s...
A novel selective and substrate-dependent synthetic protocol has been developed towards the synthesi...
Organolithium reagents effect a regioselective SN2 nucleophilic cleavage of a,ß-ethylenic epoxides o...
Herein, we report a study on the reactivity of three 1,3-diarylimidazolium-based fluoride reagents, ...
MPV type reaction In the previous note,1 we reported that Al-methanesulfonyl-diisobutylalane (DIBAO3...
International audienceThe activation of SF6, a potent greenhouse gas, under metal-free and visible l...
The development of organofluorine chemistry has revolutionised the way many agrochemical and pharmac...
The use of trialkylorganozincates and tetraalkylaluminates allows regioselective SN2 nucleophilic op...
A convenient and metal/catalyst-free approach for the reversal of regioselectivity in nucleophilic f...
A variety of epoxides undergo rapid ring opening with ammonium thiocyanate in the presence of 10 mol...