P
Peter G. Jones
Researcher at Braunschweig University of Technology
Publications - 2442
Citations - 37417
Peter G. Jones is an academic researcher from Braunschweig University of Technology. The author has contributed to research in topics: Crystal structure & Hydrogen bond. The author has an hindex of 69, co-authored 2432 publications receiving 34349 citations. Previous affiliations of Peter G. Jones include University of Cambridge & Humboldt State University.
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Darstellung von Bis-(2-chlorethyl)amino-substituierten Diazaphosphorinonen. Reversible oxidative Addition von Hexafluoraceton an σ3λ3-Phosphor-Verbindungen. Synthese von σ5λ5-Spirophosphoranen und deren Zersetzung
TL;DR: In this paper, the authors describe the reaction of 1-Methyl-pyrido[3,2-e]-3,1-oxazin-2,4-dione with benzylamines, leading to the aminonicotinic acid amides.
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VERBINDUNGEN MIT DEM 1,3-DIMETHYL-1,3- DIAZA-2-PHOSPHETIDIN-4-ON GRUNDGERüST: SYNTHESE VON 1,3-DIMETHYL-2-PHENYLIMINO- 1,3-DIAZA-2λ4-PHOSPHETIDIN-4-ON-DERIVATEN. RÖNTGENSTRUKTURANALYSE VON 4,6- DIMETHOXY -5,10-DIPHENYL-1,3,7,9- TETRAMETHYL-l,3,5,7,9,10-HEXAAZA- 4λ5,6λ55-DIPHOSPHADISPIRO[3.1.3.1]DECAN-2,8-DION
TL;DR: In this article, eine Reihe von λ3P-Diazaphosphetidinonen, MeNC(:O)N(Me)PY (Y [dbnd] NEt2: 1, N(CH2)4; 2, NPh2; 3, OMe; 4, Ncyc)2; 5), with Phenylazid wird beschrieben.
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Novel HDAC/Tubulin Dual Inhibitor: Design, Synthesis and Docking Studies of α-Phthalimido-Chalcone Hybrids as Potential Anticancer Agents with Apoptosis-Inducing Activity.
TL;DR: The trimethoxy derivative 7j showed the most potent anticancer activity, possessed the most powerful β-tubulin polymerase and HDAC 1 and 2 inhibitory activity and efficiently induced cell cycle arrest at both G2/M and preG1phases in the MCF-7 cell line.
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1,2-Azaphosphol-5-ene Complexes through Metal-Assisted Synthesis
TL;DR: In this paper, the thermal ring opening of toluene in the presence of 1-piperidino carbonitrile and various mono-and disubstituted alkenes was investigated.
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Palladium-assisted rearrangement of HC(O)C6H2(OMe)3-3,4,5 to HC(O)C6H2(OMe)3-2,3,4. X-Ray structures of [PdR(PPh3)(bipy)](CF3SO3)[R = C6H(CHO)-6,(OMe)3-2,3,4 and C6H(CHO)-2,(OMe)3-3,4,5; bipy = 2,2′-bipyridyl]
TL;DR: The anionic complex [Pd2R2Cl2(µ-Cl)2] and the neutral [pdR′2( µ-CCl) 2] were both obtained by reaction of HgR2 with appropriate palladium precursors; the isomerization of R to R′ was confirmed by X-ray studies of the derivatives [PdrR(PPh3)(bipy)](CF3SO3)5 and [PrR′(pPh3)4)5′ as discussed by the authors.