2915-44-8Relevant articles and documents
Chemistry of Tetradentate [C,N : C,N] Iminophosphorane Palladacycles: Preparation, Reactivity and Theoretical Calculations
Munín-Cruz, Paula,Ortigueira, Juan M.,Pereira, M. Teresa,Rúa-Sueiro, Marcos,Reigosa, Francisco,Vila, José M.
, p. 1190 - 1194 (2020)
A theoretical and experimental study of tetradentate [C,N : C,N] iminophosphorane palladacycles was carried out for the purpose of elucidating their behavior as compared to the parent Schiff base analogues to determine the prospect of encountering new A-frame structures for the iminophosphorane derivatives. The DFT calculations were in agreement with the experimental results regarding the performance of these ligands. New insights into the chemistry of the related dinuclear species have been obtained.
Synthesis and insecticidal activity of N,N'-bis (3-substituted thiourea) methylenedianiline derivatives
Sravanthi,Pottem, Madhusudhana Reddy,Manju
, p. 77 - 80 (2013/12/04)
Bis thiourea derivatives (5a-e) were synthesized by the treatment of diisothiocyanate (4) with various secondary amines and anilines. The structures of the compounds (5a- e) were confirmed by their spectral analysis. The insecticidal activity of the diisothicoyanate (4) and bisthiourea derivatives (5a-e) were studied and found to be better activities in comparison with the standard drug.
Size-specific ligands for RNA hairpin loops
Thomas, Jason R.,Liu, Xianjun,Hergenrother, Paul J.
, p. 12434 - 12435 (2007/10/03)
The targeting of one mRNA in the transcriptome requires small molecules that bind with substantial affinity and specificity. As such, compounds with specificity for individual RNA secondary structural motifs could be useful for targeting RNA. Described herein is the synthesis of a combinatorial library of 105 dimers of deoxystreptamine and the subsequent identification of compounds with specificity for specific RNA hairpin loop sizes, including tetraloops and octaloops. Such compounds will be useful for the perturbation of RNA function in vivo. Copyright