The past decade has witnessed the emergence of N-(acyloxy)phthalimides (NHPI esters) and its derivatives at the forefront of synthetic methods facilitating the construction of diverse molecular frameworks from the readily available carboxylic acid feedstock. The NHPI esters are predisposed to undergo reductive fragmentation via a single electron transfer (SET) process under thermal, photochemical, or electrochemical conditions to generate the corresponding carbon- or nitrogencentered radicals that participate in a multitude of synthetic transformations to forge carbon−carbon and carbon−heteroatom bonds.The chemistry involving NHPI esters has received broad applicability not only in well-designed cascade annulations but also in medicinal chemistry and natural product synthesis.
A14961922125731-81-797%
1,3-Dioxoisoindolin-2-yl 3-methylbutanoate$18.00/250mg Detail
A149620184379-71-597%
1,3-Dioxoisoindolin-2-yl 3-phenylpropanoate$71.00/1g Detail
A14961961872262-63-997%
1,3-Dioxoisoindolin-2-yl 2-ethylhexanoate$135.00/5g Detail
A14962191195529-07-797%
1,3-Dioxoisoindolin-2-yl cinnamate$85.00/5g Detail
A14962161928767-23-097%
1,3-Dioxoisoindolin-2-yl 2,2-dimethylbutanoate$36.00/1g Detail
A14961952171537-18-997%
1,3-Dioxoisoindolin-2-yl 2-methylbutanoate$40.00/1g Detail
A1496207402608-04-297%
1,3-Dioxoisoindolin-2-yl 2-(4-chlorophenyl)acetate$17.00/250mg Detail
A14961931894176-78-397%
1,3-Dioxoisoindolin-2-yl 3,3-dimethylbutanoate$25.00/250mg Detail
A14961911538551-54-097%
1,3-Dioxoisoindolin-2-yl butyrate$182.00/5g Detail
A14961972170681-06-697%
1,3-Dioxoisoindolin-2-yl 2-methylpentanoate$41.00/1g Detail
A14962061960404-19-697%
1,3-Dioxoisoindolin-2-yl 2-(4-fluorophenyl)acetate$36.00/1g Detail
A1211755126812-30-497%
1,3-Dioxoisoindolin-2-yl cyclohexanecarboxylate$538.00/25g Detail