IBX is readily reduced to IBA in the presence of molecular iodine in DMSO to generate hypoiodous acid (IOH), which reacts with a variety of olefins as well as α,β-unsaturated ketones leading to their respective iodohydrins with anti stereochemistry. The same redox chemistry in acetonitrile containing TFA produces iodonium ions for facile iodination of a variety of aromatic compounds in respectable isolated yields
International audienceThe synthesis of α‐substituted carbonyl compounds is of great importance due t...
Non‐iodinated arenes are easily and selectively converted into (diacetoxyiodo)arenes in a single ste...
This thesis discloses two different applications of hypervalent iodine(III) reagents in organic synt...
Reaction of aromatic compounds with bis(pyridine)iodonium(I) tetrafluoroborate (IPy2BF4) in the pres...
Prompted by the scant attention paid by published literature reviews to the applications of molecula...
Lodine was efficiently introduced into the methoxy substituted aromatic compounds, acetophenone, 1-i...
Aryl iodides are important synthetic intermediates that can be transformed into tritium labelled com...
An oxidative procedure for the electrophilic iodination of phenols was developed by using iodosylben...
Abstract: Some synthetic features of the IPy2BF4 reagent are presented. Among others, its utility to...
2-Iodoxybenzoic acid (IBX), a mild and efficient hypervalent iodine oxidant, has been utilised in di...
Iodination of aromatic compounds was accomplished using the procedure given by Durand, with a few sl...
The oxidative oligoazidation of phenols and ketones using iodine azide (IN3) provided by its release...
The main aim of the work presented here is to develop new, practical, economical, and environmental ...
A variety of ortho hydroxy substituted aromatic carbonyl compounds were regioselectively mono or dii...
Iodine is a special element. Its speciality lies in the fact that it is the heaviest non radioactive...
International audienceThe synthesis of α‐substituted carbonyl compounds is of great importance due t...
Non‐iodinated arenes are easily and selectively converted into (diacetoxyiodo)arenes in a single ste...
This thesis discloses two different applications of hypervalent iodine(III) reagents in organic synt...
Reaction of aromatic compounds with bis(pyridine)iodonium(I) tetrafluoroborate (IPy2BF4) in the pres...
Prompted by the scant attention paid by published literature reviews to the applications of molecula...
Lodine was efficiently introduced into the methoxy substituted aromatic compounds, acetophenone, 1-i...
Aryl iodides are important synthetic intermediates that can be transformed into tritium labelled com...
An oxidative procedure for the electrophilic iodination of phenols was developed by using iodosylben...
Abstract: Some synthetic features of the IPy2BF4 reagent are presented. Among others, its utility to...
2-Iodoxybenzoic acid (IBX), a mild and efficient hypervalent iodine oxidant, has been utilised in di...
Iodination of aromatic compounds was accomplished using the procedure given by Durand, with a few sl...
The oxidative oligoazidation of phenols and ketones using iodine azide (IN3) provided by its release...
The main aim of the work presented here is to develop new, practical, economical, and environmental ...
A variety of ortho hydroxy substituted aromatic carbonyl compounds were regioselectively mono or dii...
Iodine is a special element. Its speciality lies in the fact that it is the heaviest non radioactive...
International audienceThe synthesis of α‐substituted carbonyl compounds is of great importance due t...
Non‐iodinated arenes are easily and selectively converted into (diacetoxyiodo)arenes in a single ste...
This thesis discloses two different applications of hypervalent iodine(III) reagents in organic synt...