Tytuł artykułu
Autorzy
Wybrane pełne teksty z tego czasopisma
Identyfikatory
Warianty tytułu
Synthesis of aldehydes and ketones under solvent-free conditions. Part 1, Efficient oxidation of alcohols to aldehydes and ketones with chromium trioxide on aluminum silicate
Języki publikacji
Abstrakty
Opracowano metodę utleniania aromatycznych alkoholi do aldehydów i ketonów przez ucieranie alkoholi z tritlenkiem chromu osadzonym na krzemianie glinu bez użycia rozpuszczalnika, w temperaturze pokojowej. Wszystkie przeprowadzone reakcje kończono po 2 min. Ich wydajność wynosiła 86-96%.
Nine arom. alcs. were oxidized with CrO₃/AlSiO₃ under rubbing without any solvent at room temp. for 1-2 min to resp. aldehydes and ketones. The yield of reaction was 86-96%.
Wydawca
Czasopismo
Rocznik
Tom
Strony
2454--2456
Opis fizyczny
Bibliogr. 30 poz., tab.
Twórcy
autor
- College of Biotechnology and Bioengineering, Zhejiang University of Technology, Hangzhou 310014, China
- College of Modern Science and Technology, China Jiliang University, Hangzhou 310018, China
autor
- College of Modern Science and Technology, China Jiliang University, Hangzhou 310018, China
- Anhui Hanfang Biotechnology Co., Ltd. Huaibei 235000, China
autor
- College of Biotechnology and Bioengineering, Zhejiang University of Technology, Hangzhou 310014, China
Bibliografia
- [1] T.W.G. Solomons, C.B. Fryhle, S.A. Snyder, Organic chemistry, John Wiley & Sons, New York 2014.
- [2] M.B. Smith, March's advanced organic chemistry. Reactions, mechanisms, and structure, John Wiley & Sons, New York 2013.
- [3] H. Haines, Methods for the oxidation of organic compounds. Alcohols, alcohol derivatives, alkyl halides, nitroalkanes, alkyl azides, carbonyl compounds, hydroxyarenes and aminoarenes, Academic Press, London 1988.
- [4] L.F. Fieser, M. Fieser, Reagents for organic synthesis. Vol. 1, John Wiley & Sons, New York 1967, and subsequent volumes in the series.
- [5] F. Freeman [in:] Organic synthesis by oxidation with metal compounds (Eds. W.J. Mijs, C.R.H.I. de Jonge), Plenum Press, New York 1986.
- [6] S.V. Ley, A. Madin, Comprehensive organic synthesis, Vol. 7, (Eds. B. Trost, M.I. Fleming), Pergamon Press, London 1991.
- [7] G. Cainelli, G. Cardillo, Chromium oxidation in organic chemistry, Springer, Berlin 1984.
- [8] A. Mckillop, D.W. Young, Organic synthesis using supported reagents. Synthesis, Part 1, 401; Part 2, 481, 1979.
- [9] P. Laszlo, Preparative chemistry using supported reagents, Academic Press, San Diego 1987.
- [10] R.S. Varma, R.K. Saini, Tetrahedron Lett. 1998, 39, No. 12, 1481.
- [11] R. Kiasat, F. Kazemi, K. Nourbakhsh, Phosphorus Sulfur Silicon Rel. Elem. 2004, 179, No. 3, 457.
- [12] M.M. Heravi, N. Farhangi, Y.S. Beheshtiha, K. Assadolah, M. Ghassemzadeh, K. Tabar-Hydar, Phosphorus Sulfur Silicon Rel. Elem. 2002, 177, No. 12, 2883.
- [13] M.M. Heravi, D. Ajami, K. Tabar-Hydar, M. Ghassemzadeh, J. Chem. Res. 1999, 334.
- [14] R.S. Varma, Green Chem. 1999. 1, No. 1, 43.
- [15] J.D. Lou, Y.Y. Wu, Synth. Commun. 1987, 17, No. 14, 1717.
- [16] J.L. Lou, L.Y. Zhu, L. Wang, Monatsh. Chem. 2004, 135, 31.
- [17] L.H. Huang, J.D. Lou, L. Zhu, L. Ping, Y. Fu, Molecules 2005, 10, 778.
- [18] J.D. Lou, C. Gao, L. Li, Z. Fang, Monatsh. Chem. 2006, 137, 1071.
- [19] J.D. Lou, L.H. Huang, A.J. Marrogi, F. Li, L. Li, C. Gao, Synth. Comm. 2008, 38, No. 3, 428.
- [20] J.D. Lou, L. Li, N. Vatanian, X. Lu, X. Yu, Synth. React. Inorg. Metal Org. Nano-Metal Chem. 2008, 38, No. 4, 370.
- [21] J.D. Lou, Y.C. Ma, N. Vatanian, Q. Wang, C. Zhang, Synth. React. Inorg. Metal Org. Nano-Metal Chem. 2010, 40, No. 3, 157.
- [22] J.D. Lou, Y.C. Ma, N. Vatanian, Q. Wang, C. Zhang, Synth. React. Inorg. Metal Org. Nano-Metal Chem. 2010, 40, No. 7, 495.
- [23] J.D. Lou, J. Ge, X.N. Zou, C. Zhang, Q. Wang, Y.C. Ma, Oxid. Comm. 2011, 34, No. 2, 309.
- [24] J.D. Lou, Y.C. Ma, Q. Wang, N. Natanian, C. Zhang, Oxid. Comm. 2011, 34, No. 2, 349.
- [25] J.D. Lou, X.N. Zou, C. Zhang, Q. Wang, Y.C. Ma, Oxid. Comm. 2011, 34, No. 2, 355.
- [26] L.H. Huang, Y.C. Ma, C. Zhang, Q. Wang, X. Zou, J.D. Lou, Synth. Comm. 2012, 42, No. 22, 3377.
- [27] Y.F. Zhou, F. Lin, X.L. Lu, C. Zhang, Q. Wang, X. Zou, J.D. Lou, Oxid. Comm. 2012, 35, No. 1, 92.
- [28] J.D. Lou, F. Lin, C. Zhang, L.Y. Zhu, J. Lin, Oxid. Comm. 2013, 36, No. 2, 497.
- [29] J.D. Lou, F. Lin, C. Zhang, L.Y. Zhu, J. Lin, Oxid. Comm. 2013, 36, No. 2, 492.
- [30] J. Buckingham, Dictionary of organic compounds, Chapman & Hall, Cambridge 1996.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-d032c29a-e05f-4f53-a820-25dce220f2e1