The activation of alkenes and their subsequent functionalization is a frequently used methodology in synthetic chemistry. This review highlights recent iodine-mediated aminations and elaborates on the various strategies to bring about regio- or stereoselective transformations
Regioselective synthesis of beta-iodoethers in high yields by sonicating alkene and alcohol in the p...
With increasing demands for developing environmentally friendly synthetic approaches, hypervalent i...
The functionalization of olefins induced by chiral hypervalent iodine reagents is a basic method for...
The activation of alkenes and their subsequent functionalization is a frequently used methodology in...
Chiral hypervalent iodine compounds are used as environmentally friendly, mild, and selective oxida...
A novel and inexpensive, environmentally friendly method for the preparation of iodine monoacetate i...
Lactonizations are important steps in many synthetic sequences. Substrate-controlled reactions that ...
Lactonizations are important steps in many synthetic sequences. Substrate-controlled reactions that ...
The first stereoselective version of an iodine(III)-mediated rearrangement of arylketones in the pre...
An efficient thioamination of alkenes mediated by iodine(III) reagents is described. The use of diff...
A new chiral thiohydantoin catalyst is used for the stereoselective iodoamination of alkenes. N-iodo...
Studies to convert nitroalkanes into amides and esters using I2 and O2 revealed in situ-generated io...
A stereoselective hypervalent iodine-promoted oxidative rearrangement of 1,1-disubstituted alkenes h...
Stereoselective Rearrangements The first stereoselective version of an iodine(III)-mediated rearrang...
The thesis is divided into three sections. Section 1 describes the stereoselective preparation of 2...
Regioselective synthesis of beta-iodoethers in high yields by sonicating alkene and alcohol in the p...
With increasing demands for developing environmentally friendly synthetic approaches, hypervalent i...
The functionalization of olefins induced by chiral hypervalent iodine reagents is a basic method for...
The activation of alkenes and their subsequent functionalization is a frequently used methodology in...
Chiral hypervalent iodine compounds are used as environmentally friendly, mild, and selective oxida...
A novel and inexpensive, environmentally friendly method for the preparation of iodine monoacetate i...
Lactonizations are important steps in many synthetic sequences. Substrate-controlled reactions that ...
Lactonizations are important steps in many synthetic sequences. Substrate-controlled reactions that ...
The first stereoselective version of an iodine(III)-mediated rearrangement of arylketones in the pre...
An efficient thioamination of alkenes mediated by iodine(III) reagents is described. The use of diff...
A new chiral thiohydantoin catalyst is used for the stereoselective iodoamination of alkenes. N-iodo...
Studies to convert nitroalkanes into amides and esters using I2 and O2 revealed in situ-generated io...
A stereoselective hypervalent iodine-promoted oxidative rearrangement of 1,1-disubstituted alkenes h...
Stereoselective Rearrangements The first stereoselective version of an iodine(III)-mediated rearrang...
The thesis is divided into three sections. Section 1 describes the stereoselective preparation of 2...
Regioselective synthesis of beta-iodoethers in high yields by sonicating alkene and alcohol in the p...
With increasing demands for developing environmentally friendly synthetic approaches, hypervalent i...
The functionalization of olefins induced by chiral hypervalent iodine reagents is a basic method for...
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