Organic Letters · 2022 · 25 citations · 25 references
Natural SciencesChemistryCatalysisGreen ChemistryPhysical ChemistrySafer Chemical SynthesisSulfur ChemistryClick Chemistry
SuFEx chemistry has recently evolved as next-generation click chemistry. However, in most SuFEx syntheses, additional reagents/catalysts and carefully controlled conditions are still needed. Here, we aim to further generalize S(VI) exchange chemistry, using 4-nitrophenyl phenylmethanesulfonate as example, in which the nitrophenolate group is exchanged for a wide range of (substituted) phenols and alkyl alcohols. Quantitative yields were reached within 10 min under ambient conditions and required only filtering through silica as workup.
25
Click Chemistry in Materials Science
Weixian Xi, Timothy F. Scott, Christopher J. Kloxin et al. · Advanced Functional Materials · 2014 · 666 citations · Full text
Directing group assisted meta-hydroxylation by C–H activation
Arun Maji, Bangaru Bhaskararao, Santanu Singha et al. · Chemical Science · 2016 · 165 citations · Full text