Microencapsulated methylrhenium trioxide (MTO)/H2O2 systems for the oxidation of cardanol derivatives
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| 024 | 7 | 0 | |a 10.1351/pac200375020265 |2 doi |
| 035 | |a (NATIONALLICENCE)gruyter-10.1351/pac200375020265 | ||
| 245 | 0 | 0 | |a Microencapsulated methylrhenium trioxide (MTO)/H2O2 systems for the oxidation of cardanol derivatives |h [Elektronische Daten] |c [R. Saladino, E. Mincione, O. A. Attanasi, Paolino Filippone] |
| 520 | 3 | |a A convenient and efficient application of microencapsulated/methylrhenium trioxide (MTO) and MTO/pyridine systems for the selective oxidation of cardanol derivatives is reported. Environmentally friendly and low-cost H2O2 was used as the oxygen atom donor. The catalysts were stable systems for at least five recycling experiments. In the oxidation of C2 alkyl-substituted cardanol derivatives, high conversion and yields of the corresponding para-benzoquinones were obtained. By contrast, in the absence of the C2 substituent, an unprecedented oxidative degradation to di-γ-lactone derivative was observed. | |
| 540 | |a © 2013 Walter de Gruyter GmbH, Berlin/Boston | ||
| 700 | 1 | |a Saladino |D R. |u Dipartimento di Agrobiologia ed Agrochimica, Unità INFM, Università della Tuscia, Via S. Camillo de Lellis, 01100 Viterbo, Italy |4 aut | |
| 700 | 1 | |a Mincione |D E. |u Dipartimento di Agrobiologia ed Agrochimica, Unità INFM, Università della Tuscia, Via S. Camillo de Lellis, 01100 Viterbo, Italy |4 aut | |
| 700 | 1 | |a Attanasi |D O. A. |u Centro di Studio delle Sostanze Naturali, Università di Urbino, 61029 Urbino, Italy |4 aut | |
| 700 | 1 | |a Filippone |D Paolino |u Centro di Studio delle Sostanze Naturali, Università di Urbino, 61029 Urbino, Italy |4 aut | |
| 773 | 0 | |t Pure and Applied Chemistry |d De Gruyter |g 75/2-3(2003-01-01), 265-272 |x 0033-4545 |q 75:2-3<265 |1 2003 |2 75 |o pac | |
| 856 | 4 | 0 | |u https://doi.org/10.1351/pac200375020265 |q text/html |z Onlinezugriff via DOI |
| 908 | |D 1 |a research article |2 jats | ||
| 950 | |B NATIONALLICENCE |P 856 |E 40 |u https://doi.org/10.1351/pac200375020265 |q text/html |z Onlinezugriff via DOI | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Saladino |D R. |u Dipartimento di Agrobiologia ed Agrochimica, Unità INFM, Università della Tuscia, Via S. Camillo de Lellis, 01100 Viterbo, Italy |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Mincione |D E. |u Dipartimento di Agrobiologia ed Agrochimica, Unità INFM, Università della Tuscia, Via S. Camillo de Lellis, 01100 Viterbo, Italy |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Attanasi |D O. A. |u Centro di Studio delle Sostanze Naturali, Università di Urbino, 61029 Urbino, Italy |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Filippone |D Paolino |u Centro di Studio delle Sostanze Naturali, Università di Urbino, 61029 Urbino, Italy |4 aut | ||
| 950 | |B NATIONALLICENCE |P 773 |E 0- |t Pure and Applied Chemistry |d De Gruyter |g 75/2-3(2003-01-01), 265-272 |x 0033-4545 |q 75:2-3<265 |1 2003 |2 75 |o pac | ||
| 900 | 7 | |b CC0 |u http://creativecommons.org/publicdomain/zero/1.0 |2 nationallicence | |
| 898 | |a BK010053 |b XK010053 |c XK010000 | ||
| 949 | |B NATIONALLICENCE |F NATIONALLICENCE |b NL-gruyter | ||