Results 151 to 160 of about 38,574 (278)

Recommended dosage and environmental risk assessment of insecticides registered on main pyralid borers in China

New Plant Protection, EarlyView.
Based on the registration information of insecticides for controlling the main pyralid borers, active ingredients with high dosages were identified and analyzed based on formulations and target pests. Additionally, the environmental risks on honeybees were assessed.
Haoyu Shi, Liangang Mao, Muhammad Umair Sial, Lan Zhang, Lizhen Zhu, Chi Wu, Shankui Yuan, Yongquan Zheng, Xingang Liu   +8 more
wiley   +1 more source

Influence of Donor/Withdrawing Groups in an 3,5-Aryl-Substituted Pyrazole Organocatalyst for the Chemical Fixation of CO₂. [PDF]

ACS Omega
Oliveira Prado GET, Enes KB, Arruda da Mata ÁF, Cerqueira G, de Oliveira MAL, Costa LAS, Martins FT, Alvarenga ME, das Chagas RP, Couri MRC, Sônego Milani JL.   +10 more
europepmc   +1 more source

Halogenation of a Pyrazole Hydroazine Vat Dye

, 1967
Yoshio NAGAI, Jirô KIMIJIMA, Nobuyuki GOTOH   +2 more
openalex   +2 more sources

Studies in Heterocyclic Compounds. Part X. Synthesis and Antibacterical Study of Some New 3, 5-Diaryl-4- (Substituted Sulphonamidobenzeneazo) Pyrazoles [PDF]

, 1976
AJAYA KABRA, G. S. SAHARIA, Himanshi Sharma   +2 more
openalex   +1 more source

Penta‐ and Hexacoordinated Copper(II) Complexes with Azido and 4‐amino‐3,5‐di‐2‐pyridyl‐4H‐1,2,4‐triazole Ligands with Field‐Induced Slow Magnetic Relaxation

ChemistryOpen, EarlyView.
A field‐induced slow magnetic relaxation was observed in an ionic pentacoordinated Cu(II) complex with 4‐amino‐3,5‐di‐2‐pyridyl‐4H‐1,2,4‐triazole and azido ligands. The analysis of the relaxation behaviour supports the origin of the slow magnetic relaxation in intramolecular low‐energy vibration modes participating in the one‐phonon direct and two ...
Svitlana Vitushkina, Ivan Potočňák, Oleksandr Bukrynov, Lucia Váhovská, Mariia Holub, Erik Čižmár   +5 more
wiley   +1 more source

Synthetic chemistry enabling the discovery and development of a series of pyrazoles as HPK1 inhibitors. [PDF]

RSC Med Chem
Metrano AJ, Morrill LA, Bommakanti G, Casella R, Cook S, Escobar RA, Giblin KA, Gosselin E, Grebe T, Hariparsad N, Howells R, Lamont GM, Mele DA, Pflug A, Proia TA, Rezaei H, Richter M, Richards R, San Martin M, Schimpl M, Schuller AG, Sha L, Sheppeck JE, Song K, Tang H, Wagner DJ, Wang J, Wu A, Wu D, Wu Y, Xu K, Ye M, Shields JD, Grimster NP.   +33 more
europepmc   +1 more source

Studies in Heterocyclic Compounds. Part XIII. Synthesis of some new 3, 5-Diaryl-4-(substituted sulphonamidobenzeneazo) pyrazoles as Potential Antimicrobial Agents [PDF]

, 1976
H. C. MUTREJA, G. S. SAHARIA, H. R. SHARMA   +2 more
openalex   +1 more source

Evaluation of the Antifungal Properties of Azomethine‐Pyrazole Derivatives from a Structural Perspective

ChemistryOpen, EarlyView.
A series of azomethine‐pyrazole derivatives bearing a para‐substituted azo‐phenyl ring is straightforwardly prepared. The new compounds display an elevated antifungal activity against various Candida species and Cryptococcus neoformans strains. DFT and molecular docking calculations are used to determine possible routes of action through interactions ...
María Isabel Murillo, Andrés Camilo Restrepo‐Acevedo, Cristian Rocha‐Roa, Susana Zacchino, Laura Svetaz, Simón Hernández‐Ortega, Rodrigo Abonia, Ronan Le Lagadec, Fernando Cuenú‐Cabezas   +8 more
wiley   +1 more source

Unraveling aromaticity: the dual worlds of pyrazole, pyrazoline, and 3D carborane. [PDF]

Beilstein J Org Chem
Noori Z, Solà M, Viñas C, Teixidor F, Poater J.   +4 more
europepmc   +1 more source

The Ring Contraction of Pyridazinones to Pyrazoles. VI

, 1972
Yoshifumi Maki, M. TAKAYA
openalex   +2 more sources