32162-27-9Relevant academic research and scientific papers
Synthesis, characterization, magnetic and catalytic properties of a ladder-shaped MnII coordination polymer
Lymperopoulou, Smaragda,Papastergiou, Maria,Louloudi, Maria,Raptopoulou, Catherine P.,Psycharis, Vassilis,Milios, Constantinos J.,Plakatouras, John C.
, p. 3638 - 3644 (2014/08/18)
[Mn(LH)(H2O)]n {1, where LH2- is the dianion of N-(4-carboxybenzyl)iminodiacetic acid} has been synthesized and its crystal structure has been determined. The crystal of 1 is built from 1D polymeric ladder-shaped chains that extend to a 3D supramolecular architecture through H-bonds. The compound was characterized with spectroscopic and physicochemical techniques. Variable-temperature magnetic data suggest that there are weak antiferromagnetic interactions. Compound 1 has been evaluated as a heterogeneous oxidation catalyst. It catalyzes alkene epoxidation selectively in relatively high yields. Copyright
Opening of epoxide rings catalyzed by niobium pentachloride
Constantino, Mauricio Gomes,Lacerda Jr., Valdemar,Invernize, Paulo Roberto,Filho, Luiz Carlos Da Silva,Da Silva, Gil Valdo Jose
, p. 3529 - 3539 (2008/03/13)
The behavior of several epoxides when treated with NbCl5 was studied. In general, the studied epoxides reacted rapidly with NbCl5, giving, in most cases, more than one product (chlorohydrins, products containing solvent residues, as well as rearrangement products). A detailed study was performed to verify the effects of the temperature (rt, 0°C, or -78°C) and of the NbCl5 molar concentration on the composition of the products, yield, and time required for the reactions. Copyright Taylor & Francis Group, LLC.
Diastereoselective epoxidation of olefins by organo sulfonic peracids, II
Kluge,Schulz,Liebsch
, p. 2957 - 2976 (2007/10/03)
We have investigated the behaviour of sulfonic peracids 2 in situ generated towards olefins 7a, 7b, 9, 11, 14, 16, 18, allylic acid and homoallylic alcohols 20, 22, 24, 26, 28, 30, 33 and α,β-unsaturated ketones 35, 37, 39. Generally, the epoxidation proceeds in a peracid-like manner with greater diastereoselectivity than those by common oxidants. In particular, the epoxidation of Δ4 3-ketosteroids 39a-i led to 4α,5α-epoxides 40a-i with remarkable high de-values. Enhanced α-selectivity was also found in the epoxidation of cholesterol 28b. Due to the mild reaction conditions, even acid sensitive epoxides 8a, 8b, 10, 12, 13, 15, 17, 19 were obtained in good yields.
Photooxygenation of olefins in the presence of titanium(IV) catalyst: A convenient 'one-pot' synthesis of epoxy alcohols
Adam,Braun,Griesbeck,Lucchini,Staab,Will
, p. 203 - 212 (2007/10/02)
The photooxygenation of olefins in the presence of transition-metal complexes derived from Ti, V, and Mo constitutes a convenient and efficient 'one-pot' synthesis of epoxy alcohols. First, singlet oxygen transforms the olefin via an ene reaction into its allylic hydroperoxide, and subsequently, the allylic hydroperoxide is converted via transition-metal-catalyzed oxygen transfer into its epoxy alcohol. From the point of view of the olefinic substrate, the oxygen transfer is intermolecular, one allylic hydroperoxide molecule serving as oxygen donor and the other as oxygen acceptor in the form of its allylic alcohol, the transition metal playing the role of a template for both as in the Sharpless epoxidation. Unlike the latter process, the hydroperoxide donor and the allylic alcohol acceptor are generated in situ and continually consumed via a novel oxygen-transfer chain sequence.
Stereocontrolled Regiospecificity of the Water Loss from trans-Sobrerol Radical Cation upon Electron Ionization
Selva, Antonio,Ferrario, Francesco,Ventura, Paolo,Pellegata, Renato
, p. 523 - 529 (2007/10/02)
Water loss from trans-sobrerol upon electron impact ionization selectively involves the tertiary OH group, predominantly occuring by a stereocontrolled H-transfer from C(5) position in a rate-determining step process, as proved by 18O and deuterium labelling.Monomethyl ethers behave accordingly.Ionic structures of the water-loss product or products are investigated by metastable ion and collision activation mass-analysed ion kinetic energy spectroscopy, using model ions generated from some substrates, which are chemically related to trans-sobrerol in condensed phase, i.e. α-pinane epoxide, cis-sobrerol and pinol.A substantial conversion of cis-sobrerol molecular ions to ionized pinol by loss of water has been demonstrated.
NaOCl OLEFIN EPOXIDATIONS CATALYZED BY Mn-PORPHYRINS UNDER TWO-PHASE CONDITIONS. INFLUENCE OF STRUCTURAL FACTORS ON THE STABILITY, CATALYTIC ACTIVITY AND SELECTIVITY OF PORPHYRINS
Banfi, Stefano,Montanari, Fernando,Penso, Michele,Sosnovskikh, Viecheslav,Vigano, Patrizia
, p. 689 - 694 (2007/10/02)
The progressive deactivation of a series of Mn-tetraarylporphyrins (TPP, TMP, TAP, TPFPP, TDClPP), which are very efficient catalysts for olefin epoxidations, has been measured under the reaction conditions.Reactions are carried out at 0 deg C in CH2Cl2-H2O, with NaOCl aqueous solution at pH 9.5, in the presence of N-hexyl imidazole as an axial ligand and, generally, of a phase-transfer catalyst.All porphyrins are more or less rapidly deactivated, the only exception being Mn-TDClPP which can be almost quantitatively recovered.Both steric and electronic effects seem therefore to be essential for the chemical stability of metallo-porphyrins.In the presence of 0.005 molar equivalents of Mn-TDClPP, α-olefins and sterically unhindered internal olefins are epoxidized in high yields at 0 deg C and very short reaction times.Highly regio- and stereo-selective oxidations can be also achieved.
