Elsevier eBooks, Journal Year: 2024, Volume and Issue: unknown, P. 365 - 391
Published: Nov. 15, 2024
Language: Английский
Elsevier eBooks, Journal Year: 2024, Volume and Issue: unknown, P. 365 - 391
Published: Nov. 15, 2024
Language: Английский
ACS Catalysis, Journal Year: 2024, Volume and Issue: unknown, P. 15221 - 15236
Published: Oct. 2, 2024
Language: Английский
Citations
2Journal of the American Chemical Society, Journal Year: 2024, Volume and Issue: 146(46), P. 31391 - 31399
Published: Nov. 12, 2024
The alkene-carboxylate transposition (ACT) of allyl carboxylates is one the most atom-economic and synthetically reliable transformations in organic chemistry, as are versatile synthetic intermediates. Classic ACT transformations, including [3,3]-sigmatropic rearrangement transition metal-catalyzed allylic rearrangement, typically yield 1,2-alkene/1,3-acyloxy shifted products through a two-electron process. However, position-altered to produce distinct 1,3-alkene/1,2-acyloxy remains elusive. Here, we report first cobalt-hydride-catalyzed carboxylates, enabling access these unprecedented via 1,2-radical migration (RaM) strategy. This transformation demonstrates broad functional group tolerance, suitable for late-stage modification complex molecules, amenable gram-scale synthesis. It also expands reaction profiles both cobalt catalysis. Preliminary experimental computational studies suggest mechanism involving metal-hydride hydrogen atom transfer (MHAT) 1,2-RaM expected serve basis development Co-H-catalyzed generating wide array valuable building blocks synthetic, medicinal, materials chemistry.
Language: Английский
Citations
2Journal of Catalysis, Journal Year: 2024, Volume and Issue: 440, P. 115846 - 115846
Published: Nov. 13, 2024
Language: Английский
Citations
2Molecular Catalysis, Journal Year: 2024, Volume and Issue: 568, P. 114462 - 114462
Published: Aug. 28, 2024
Language: Английский
Citations
1Plasma Science and Technology, Journal Year: 2024, Volume and Issue: 26(7), P. 075510 - 075510
Published: April 1, 2024
Abstract Catalysis of molecular radicals is often performed in interesting experimental configurations. One possible configuration tubular geometry. The are introduced into the tubes on one side, and stable molecules exhausted other side. penetration depth depends numerous parameters, so it not always feasible to calculate it. This article presents systematic measurements oxygen atoms along made from nickel, cobalt, copper. source O was a surfatron-type microwave plasma. initial density depended gas flow 0.7×10 21 m −3 , 2.4×10 4.2×10 at rates 50, 300, 600 sccm, pressures 10, 35, 60 Pa, respectively. temperature remained room throughout experiments. dissociation fraction decreased exponentially length all cases. depths for well-oxidized nickel were 1.2, 1.7, 2.4 cm, For they slightly lower 1.0, 1.3, 1.6 respectively, while copper, 1.1, 1.7 results explained by dynamics heterogeneous surface association. These data useful any attempt estimate loss fragments tubes, which serve as catalysts association various molecules.
Language: Английский
Citations
0Research Square (Research Square), Journal Year: 2024, Volume and Issue: unknown
Published: Aug. 2, 2024
Language: Английский
Citations
0Research Square (Research Square), Journal Year: 2024, Volume and Issue: unknown
Published: Aug. 7, 2024
Language: Английский
Citations
0Elsevier eBooks, Journal Year: 2024, Volume and Issue: unknown, P. 365 - 391
Published: Nov. 15, 2024
Language: Английский
Citations
0