The title compound {systematic name: 2-[(3,5-dimenthylpyrazol-1-yl)meth-yl]isoindole-1,3-dione}, C(14)H(13)N(3)O(2), was prepared by reaction of N-(bromo-meth-yl)phthalimide and 3,5-dimethyl-pyrazole in chloro-form solution. The mol-ecular structure and packing are stabilized by intra-molecular C-H⋯O hydrogen-bonding and C-H⋯π inter-actions.

In the title compound, C13H12N2O5, the phthalimide ring system is essentially planar, with a maximum deviation of 0.0479 (14) Å. In the crystal, each mol-ecule is linked via six neighbouring mol-ecules into a three-dimensional network through N-H⋯O and O-H⋯O hydrogen bonds, which form an R 3 (2)(8) ring motif.

Hydrogen-bond-mediated complexation of a CG base pair by a hexylureido phthalimide and a hexylureido isoindolin-1-one was studied by (1)H NMR spectroscopy in an organic solvent. Chemical shift data indicate that both receptors effectively bind the CG base pair from the major groove side.

4,5-Bis(aminomethyl)acridine, useful as an immunosuppressant, was prepared in 31% overall yield by the reaction of acridine with N-(hydroxymethyl)phthalimide and subsequent decomposition with excess 6 N HCl. The drug was found to produce a suppression of the humoral antibody response comparable to several known immunosuppressive agents.

In the field of organosulfur chemistry, sulfenylating agents are an important key in C–S bond formation strategies. Among various precursors, N -sulfenylsuccinimide/phthalimide derivatives have shown highly electrophilic reactivity for asymmetric synthesis many organic compounds. Hence, this review article, we focus on application these alternative reagents transformations.

A series of N-ethyl phthalimide esters 4(a-n) were synthesized and characterized by spectroscopic studies. Further, the molecular structure of majority of compounds were analysed by single crystal X-ray diffraction studies. The X-ray analysis revealed the importance of substituents on the crystal stability and molecular packing. All the synthesized compounds were tested for in vitro antioxidant...

Catalytic transformations involving Pd s-alkyl or s-aryl intermediates are widely used in organic synthesis and offer attractive routes to many valuable products. However, the vast majority of these reactions proceed by Pd/Pd mechanisms. As a result, the diversity of structures/bonds that can be constructed is constrained by the limitations of this redox cycle. Recent studies have explored the ...