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
Non‐iodinated arenes are easily and selectively converted into (diacetoxyiodo)arenes in a single ste...
Lodine was efficiently introduced into the methoxy substituted aromatic compounds, acetophenone, 1-i...
Studies to convert nitroalkanes into amides and esters using I2 and O2 revealed in situ-generated io...
The activation of alkenes and their subsequent functionalization is a frequently used methodology in...
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 ...
Stereoselective Rearrangements The first stereoselective version of an iodine(III)-mediated rearrang...
An efficient thioamination of alkenes mediated by iodine(III) reagents is described. The use of diff...
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...
Chiral hypervalent iodine compounds are used as environmentally friendly, mild, and selective oxida...
The functionalization of olefins induced by chiral hypervalent iodine reagents is a basic method for...
A new chiral thiohydantoin catalyst is used for the stereoselective iodoamination of alkenes. N-iodo...
A procedure for the iodoamination of unfunctionalized olefins tethered to a tosyl-protected NH-group...
Novel electron-deficient chiral hypervalent iodine reagents were prepared in good overall yields. Th...
Non‐iodinated arenes are easily and selectively converted into (diacetoxyiodo)arenes in a single ste...
Lodine was efficiently introduced into the methoxy substituted aromatic compounds, acetophenone, 1-i...
Studies to convert nitroalkanes into amides and esters using I2 and O2 revealed in situ-generated io...
The activation of alkenes and their subsequent functionalization is a frequently used methodology in...
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 ...
Stereoselective Rearrangements The first stereoselective version of an iodine(III)-mediated rearrang...
An efficient thioamination of alkenes mediated by iodine(III) reagents is described. The use of diff...
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...
Chiral hypervalent iodine compounds are used as environmentally friendly, mild, and selective oxida...
The functionalization of olefins induced by chiral hypervalent iodine reagents is a basic method for...
A new chiral thiohydantoin catalyst is used for the stereoselective iodoamination of alkenes. N-iodo...
A procedure for the iodoamination of unfunctionalized olefins tethered to a tosyl-protected NH-group...
Novel electron-deficient chiral hypervalent iodine reagents were prepared in good overall yields. Th...
Non‐iodinated arenes are easily and selectively converted into (diacetoxyiodo)arenes in a single ste...
Lodine was efficiently introduced into the methoxy substituted aromatic compounds, acetophenone, 1-i...
Studies to convert nitroalkanes into amides and esters using I2 and O2 revealed in situ-generated io...
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