Inorganic Chemistry Communications, Journal Year: 2024, Volume and Issue: unknown, P. 113799 - 113799
Published: Dec. 1, 2024
Language: Английский
Inorganic Chemistry Communications, Journal Year: 2024, Volume and Issue: unknown, P. 113799 - 113799
Published: Dec. 1, 2024
Language: Английский
Electrochimica Acta, Journal Year: 2024, Volume and Issue: 502, P. 144860 - 144860
Published: Aug. 8, 2024
Language: Английский
Citations
9Inorganic Chemistry Communications, Journal Year: 2024, Volume and Issue: 168, P. 112989 - 112989
Published: Aug. 15, 2024
Language: Английский
Citations
4Journal of Molecular Structure, Journal Year: 2024, Volume and Issue: unknown, P. 139919 - 139919
Published: Sept. 1, 2024
Language: Английский
Citations
4Bioorganic Chemistry, Journal Year: 2025, Volume and Issue: 156, P. 108202 - 108202
Published: Jan. 22, 2025
Language: Английский
Citations
0Next research., Journal Year: 2025, Volume and Issue: unknown, P. 100188 - 100188
Published: Feb. 1, 2025
Language: Английский
Citations
0Sustainable Energy Technologies and Assessments, Journal Year: 2024, Volume and Issue: 73, P. 104104 - 104104
Published: Nov. 23, 2024
Language: Английский
Citations
3Alexandria Engineering Journal, Journal Year: 2024, Volume and Issue: 108, P. 654 - 661
Published: Sept. 19, 2024
Language: Английский
Citations
2International Journal of Biological Macromolecules, Journal Year: 2024, Volume and Issue: 280, P. 136058 - 136058
Published: Sept. 26, 2024
Language: Английский
Citations
2Journal of the American Chemical Society, Journal Year: 2024, Volume and Issue: unknown
Published: Dec. 12, 2024
β-Amino acids serve as crucial building blocks for a broad range of biologically active molecules and peptides with potential peptidomimetics. While numerous methods have been developed the synthesis β-amino acids, most them require multistep preparation specific reagents substrates, which limits their synthetic practicality. In this regard, homologative transformation abundant readily available α-amino would be an attractive approach acid synthesis. Herein, we disclose development sequential process to provide diverse from derivatives commercially phosphonium ylides via visible light photoredox catalysis. two-step protocol, function bifunctional linchpin: they act carbon nucleophile forge C-C bond in first step carbon-centered radical source modifications scaffold second step. The orthogonal activation these reactivities under mild photocatalytic conditions enables modular three-component assembly access dipeptides high structural diversity.
Language: Английский
Citations
2Journal of Applied Polymer Science, Journal Year: 2024, Volume and Issue: 141(42)
Published: Aug. 16, 2024
Abstract Phthalonitrile monomer containing oxazine ring (BPS‐Ph) was synthesized using bisphenol‐S, aniline, paraformaldehyde, and 4‐nitrophthalonitrile via a two‐step method. The differential scanning calorimetry (DSC) data of the curing process BPS‐Ph indicates that peak polymerization temperature cyan group is about 250°C confirms promoting effect on reaction phthalonitrile. rheological E51/DDS also has process. activation energy studied iso‐conversional method principle. corresponding to crosslinking 75.79 60.54 kJ mol −1 , respectively, for pure E51/DDS/BPS‐Ph. Moreover, phthalhydrazine 74.1 which rather lower than in BPS‐Ph, implies synergistically catalytic amine. addition significantly improves thermal behaviors thermoset. char yield N 2 atmosphere increased from 15.6% 53.9% when adding 30% E51/DDS. weight loss decreased 407 385°C. phase separation size poly‐BPS‐Ph tens hundreds nanometers according atomic force microscopy (AFM) diagram. It indicated incorporation phthalonitrile into epoxy/amine system an applicable effective way promote behavior
Language: Английский
Citations
1