Tetrabutylammonium fluoride (1) catalyses under mild conditions the opening of epoxides 2a-k with thiols 3-6 to produce the corresponding beta-hydroxy thioethers 7-11 in excellent yields (88-100%) and with high regioselectivity. Furthermore, O-protected glycidols react without any loss of the protective group
S-Alkylisothiouronium salt as a nontoxic,odorless and simply operational alternative of thiol was re...
Borinic acid catalysis has been used by our group to effect ring-opening and rearrangement reactions...
Regioselective opening of the thiirane ring occurs spontaneously with Group IV B organometallics suc...
N-Bromosuccinimide (NBS) catalyses the ring opening of various epoxides with different thiols in CH3...
Tetrabutylammonium dihydrogentrifluoride, Bu(4)N(+)H(2)F(3)(-), was found to be a very efficient cat...
The regioselective opening of epoxides with organotin oxides 1 and 2, in presence of halogenated alc...
A simple efficient, stereoselective, and highly regioselective method for the synthesis of beta-hydr...
A highly effective protocol for ring opening of epoxides with allyl and propargyl alcohols, aniline ...
The regiochem. outcome of the ring-opening of epoxides bearing remote polar functionalities was esta...
We found that the ring-opening fluorination of terminal epoxidesusing TBABF-KHF2 proceeds with high ...
Titanium tetrachloride promoted reaction of silyl ketene acetals with epoxides, followed by acidic w...
Spiro epoxides 2 derived from glucose can be opened either in acidic or basic conditions with opposi...
Efficient ring opening of 3,4-epoxyesters with alcohols to produce 4-alkoxy-3-hydroxyesters and thei...
A variety of epoxides underwent facile cleavage by thiols under the catalysis of 1-methyl-3-butylimi...
Tetrathiomolybdate provides an easy access to \beta-hydroxy disulfides, \beta-hydroxy sulfides, and ...
S-Alkylisothiouronium salt as a nontoxic,odorless and simply operational alternative of thiol was re...
Borinic acid catalysis has been used by our group to effect ring-opening and rearrangement reactions...
Regioselective opening of the thiirane ring occurs spontaneously with Group IV B organometallics suc...
N-Bromosuccinimide (NBS) catalyses the ring opening of various epoxides with different thiols in CH3...
Tetrabutylammonium dihydrogentrifluoride, Bu(4)N(+)H(2)F(3)(-), was found to be a very efficient cat...
The regioselective opening of epoxides with organotin oxides 1 and 2, in presence of halogenated alc...
A simple efficient, stereoselective, and highly regioselective method for the synthesis of beta-hydr...
A highly effective protocol for ring opening of epoxides with allyl and propargyl alcohols, aniline ...
The regiochem. outcome of the ring-opening of epoxides bearing remote polar functionalities was esta...
We found that the ring-opening fluorination of terminal epoxidesusing TBABF-KHF2 proceeds with high ...
Titanium tetrachloride promoted reaction of silyl ketene acetals with epoxides, followed by acidic w...
Spiro epoxides 2 derived from glucose can be opened either in acidic or basic conditions with opposi...
Efficient ring opening of 3,4-epoxyesters with alcohols to produce 4-alkoxy-3-hydroxyesters and thei...
A variety of epoxides underwent facile cleavage by thiols under the catalysis of 1-methyl-3-butylimi...
Tetrathiomolybdate provides an easy access to \beta-hydroxy disulfides, \beta-hydroxy sulfides, and ...
S-Alkylisothiouronium salt as a nontoxic,odorless and simply operational alternative of thiol was re...
Borinic acid catalysis has been used by our group to effect ring-opening and rearrangement reactions...
Regioselective opening of the thiirane ring occurs spontaneously with Group IV B organometallics suc...
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