5-Endo-dig iodocyclisations of alk-3-yn-1,2-diols 4, followed by in situ dehydration, lead to good yields of β-iodofurans 5, which can subsequently be converted into a wide range of derivatives 6-13, using transition metal-catalysed coupling reactions or halogen-metal exchange
Iodocyclization of 2-allylphenols is a suitable method to access furans and dihydrofurans with adequ...
A strategy for the synthesis of spiroketal compounds through a tandem iodocyclization of 1-(2-ethyny...
Palladium-catalyzed highly regioselective 5-exo-dig O-cyclization/coupling of a series of ethyl 3-(2...
5-endo-dig cyclisations of 3-alkyne-1,2-diols using iodine as the electrophile proceed smoothly to d...
A library of furans has been synthesized by iodocyclization and further diversified by palladium-cat...
Tetrahydrofuran derivatives can be obtained by cyclo-functionalization of homoallylic alcohols beari...
An efficient synthesis of a variety of dibenzofuran derivatives via Cu-catalyzed cyclization diaryli...
5-endo-Iodocyclisations of stereoisomers of 3-alkene-1,2-diols 9, 12, 15 and 18 are stereoselective ...
A strategy for the synthesis of 6,9-dihydropyrido[1,2-<i>a</i>]indoles through a cascade iodocycli...
Overall 5-endo-trig iodocyclizations of homoallylic alcohols, with a range of substitution patterns,...
Iodocyclization of 2-allylphenols is a suitable method to access furans and dihydrofurans with adequ...
Synthesis of highly substituted 3-fluorofurans is reported. The sequence began with preparation of t...
Iodoetherification of the (Z)-3-hydroxy-5-alkenoates 4 leads exclusively to the hydroxytetrahydrofur...
Reductive homocoupling of alkyl and aryl halides in presence of indium metal in DMF produces bialkyl...
Methodologies based on the electrophilic halocyclization of γ-unsaturated alcohols to tetrahydrohyfu...
Iodocyclization of 2-allylphenols is a suitable method to access furans and dihydrofurans with adequ...
A strategy for the synthesis of spiroketal compounds through a tandem iodocyclization of 1-(2-ethyny...
Palladium-catalyzed highly regioselective 5-exo-dig O-cyclization/coupling of a series of ethyl 3-(2...
5-endo-dig cyclisations of 3-alkyne-1,2-diols using iodine as the electrophile proceed smoothly to d...
A library of furans has been synthesized by iodocyclization and further diversified by palladium-cat...
Tetrahydrofuran derivatives can be obtained by cyclo-functionalization of homoallylic alcohols beari...
An efficient synthesis of a variety of dibenzofuran derivatives via Cu-catalyzed cyclization diaryli...
5-endo-Iodocyclisations of stereoisomers of 3-alkene-1,2-diols 9, 12, 15 and 18 are stereoselective ...
A strategy for the synthesis of 6,9-dihydropyrido[1,2-<i>a</i>]indoles through a cascade iodocycli...
Overall 5-endo-trig iodocyclizations of homoallylic alcohols, with a range of substitution patterns,...
Iodocyclization of 2-allylphenols is a suitable method to access furans and dihydrofurans with adequ...
Synthesis of highly substituted 3-fluorofurans is reported. The sequence began with preparation of t...
Iodoetherification of the (Z)-3-hydroxy-5-alkenoates 4 leads exclusively to the hydroxytetrahydrofur...
Reductive homocoupling of alkyl and aryl halides in presence of indium metal in DMF produces bialkyl...
Methodologies based on the electrophilic halocyclization of γ-unsaturated alcohols to tetrahydrohyfu...
Iodocyclization of 2-allylphenols is a suitable method to access furans and dihydrofurans with adequ...
A strategy for the synthesis of spiroketal compounds through a tandem iodocyclization of 1-(2-ethyny...
Palladium-catalyzed highly regioselective 5-exo-dig O-cyclization/coupling of a series of ethyl 3-(2...
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