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1. Preparation and Characterization of N , N′ ‐Dialkyl‐1,3‐propanedialdiminium Chlorides, N , N′ ‐Dialkyl‐1,3‐propanedialdimines, and Lithium N , N′ ‐Dialkyl‐1,3‐propanedialdiminates

   https://doi.org/10.1002/hlca.202200152  

   Schmit, Claire E.; Girolami, Gregory S. (May 2023, Helvetica Chimica Acta)
2. Tuning N , N -Diarylanilinosquaraine Crystal Packing: n -Hexylaryl and Fluoroaryl Substitution

   https://doi.org/10.1021/acs.cgd.8b01621  

   Schlueter, John A.; Homnick, Paul J.; Della Pelle, Andrea M.; Lahti, Paul M.; Thayumanavan, S. (May 2019, Crystal Growth & Design)
3. N , N -Disubstituted- N ′-acylthioureas as modular ligands for deposition of transition metal sulfides

   https://doi.org/10.1039/c7dt04860b  

   Ali, Zahra; Richey, Nathaniel E.; Bock, Duane C.; Abboud, Khalil A.; Akhtar, Javeed; Sher, Muhammad; McElwee-White, Lisa (January 2018, Dalton Transactions)

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   First row transition metal complexes (Ni, Co, Cu, Zn) with N , N -disubstituted- N ′-acylthiourea ligands have been synthesized and characterized. Bis( N , N -diisopropyl- N ′-cinnamoylthiourea)nickel was found to have the lowest onset temperature for thermal decomposition. Thin film deposition of Ni, Co, and Zn sulfides by aerosol assisted chemical vapor deposition from their respective N , N -diisopropyl- N ′-cinnamoylthiourea complexes at 350 °C has been demonstrated. 

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4. Crystal structure of N , N -diisopropyl-4-methylbenzenesulfonamide

   https://doi.org/10.1107/S2056989020007185  

   Stenfors, Brock A.; Staples, Richard J.; Biros, Shannon M.; Ngassa, Felix N. (July 2020, Acta Crystallographica Section E Crystallographic Communications)

   The synthesis of the title compound, C 13 H 21 NO 2 S, is reported here along with its crystal structure. This compound crystallizes with two molecules in the asymmetric unit. The sulfonamide functional group of this structure features S=O bond lengths ranging from 1.433 (3) to 1.439 (3) Å, S—C bond lengths of 1.777 (3) and 1.773 (4) Å, and S—N bond lengths of 1.622 (3) and 1.624 (3) Å. When viewing the molecules down the S—N bond, the isopropyl groups are gauche to the aromatic ring. On each molecule, two methyl hydrogen atoms of one isopropyl group are engaged in intramolecular C—H...O hydrogen bonds with a nearby sulfonamide oxygen atom. Intermolecular C—H...O hydrogen bonds and C—H...π interactions link molecules of the title compound in the solid state. 

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5. Transition Metal‐Free Aroylation of Diarylmethanes with N ‐Bn‐ N ‐Boc Arylamides and N ‐Acylpyrroles

   https://doi.org/10.1002/adsc.202000622  

   Yang, Fan; Zou, Dong; Chen, Shuguang; Wang, Huan; Zhao, Yichen; Zhao, Liyi; Li, Linlin; Li, Jie; Walsh, Patrick J. (August 2020, Advanced Synthesis & Catalysis)

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