TY - JOUR
T1 - Reactivity and Applications of Iodine Monochloride in Synthetic Approaches
AU - Day, David P.
AU - Alsenani, Nawaf I.
AU - Alsimaree, Abdulrahman A.
N1 - Publisher Copyright:
© 2021 Wiley-VCH GmbH
PY - 2021/8/13
Y1 - 2021/8/13
N2 - Over the last half-decade, routes towards accessing halogenated compounds of value such as bioactive pharmaceuticals, organic building blocks has been of interest to the synthetic community. The demand for new methodologies to access important compounds has surged over the period. Amongst the halogenating agents available in a chemist's toolbox, one reagent in particular, iodine monochloride (ICl), is relatively under employed in comparison to alternatives such as molecular iodine for example. In this Minireview, we document the most recent applications (2015–2020) of ICl in synthetic organic transformations, namely halogenations including iodinations and chlorination reactions, cyclizations, metathesis reactions as well as oxidation processes. Furthermore, its versatile nature and interesting properties will be discussed, through its advantages and downfalls over other halogenating reagents, and discussions where relevant to compare modes of reactivity and mechanistic insights is presented.
AB - Over the last half-decade, routes towards accessing halogenated compounds of value such as bioactive pharmaceuticals, organic building blocks has been of interest to the synthetic community. The demand for new methodologies to access important compounds has surged over the period. Amongst the halogenating agents available in a chemist's toolbox, one reagent in particular, iodine monochloride (ICl), is relatively under employed in comparison to alternatives such as molecular iodine for example. In this Minireview, we document the most recent applications (2015–2020) of ICl in synthetic organic transformations, namely halogenations including iodinations and chlorination reactions, cyclizations, metathesis reactions as well as oxidation processes. Furthermore, its versatile nature and interesting properties will be discussed, through its advantages and downfalls over other halogenating reagents, and discussions where relevant to compare modes of reactivity and mechanistic insights is presented.
KW - Cyclization
KW - Iodination
KW - Iodine Monochloride Chlorination
KW - Oxidation
UR - http://www.scopus.com/inward/record.url?scp=85108323737&partnerID=8YFLogxK
U2 - 10.1002/ejoc.202100554
DO - 10.1002/ejoc.202100554
M3 - Review article
AN - SCOPUS:85108323737
VL - 2021
SP - 4299
EP - 4307
JO - European Journal of Organic Chemistry
JF - European Journal of Organic Chemistry
SN - 1434-193X
IS - 30
ER -