10.1002/anie.201908451
Angewandte Chemie International Edition
RESEARCH ARTICLE
[1]
T. Ostermann in Building Blocks for the Feed Industry: Oxea Expands
Production Capabilities for Butyric Acid and Propionic Acid, OXEA
GmbH, Monheim am Rhein, 2017.
[34] E. Drent, L. Petrus, S. A. J. van Langen in Process for the
carbonylation of olefinically unsaturated compounds with a palladium
catalyst. Pantent EP0282142, 1987.
[2]
[3]
[4]
[5]
G. A. Burdock in Fenaroli's Handbook of Flavor Ingredients, CRC Press,
Boca Raton, 2009.
[35] E. Drent, E. Kragtwijk in Process for the carbonylation of olefin. Pantent
EP0495548, 1991.
S. H. Hoseinifar, Y.-Z. Sun, C. M. Caipang, Aquacult. Res. 2017, 48,
1380-1391.
[36] E. Drent, P. Arnoldy, P. H. M. Budzelaar, J. Organomet. Chem. 1993,
455, 247-253.
N. Ruiz-Lopez, R. P. Haslam, J. A. Napier, O. Sayanova, Plant J. 2014,
77, 198-208.
[37] E. Drent, P. Arnoldy, P. H. M. Budzelaar, J. Organomet. Chem. 1994,
475, 57-63.
G. V. Polycarpo, I. Andretta, M. Kipper, V. C. Cruz-Polycarpo, J. C.
Dadalt, P. H. M. Rodrigues, R. Albuquerque, Poult. Sci. 2017, 96, 3645-
3653.
[38] R. I. Pugh, E. Drent, P. G. Pringle, Chem. Commun. 2001, 1476-1477.
[39] L. Crawford, D. J. Cole-Hamilton, E. Drent, M. Bühl, Chem. Eur. J. 2014,
20, 13923-13926.
[6]
[7]
[8]
V. L. Bagal, V. K. Khatta, B. S. Tewatia, S. K. Sangwan, S. S. Raut, Vet.
World, 2016, 9, 377-382.
[40] M. van Meur, J. D. Nobbs, C. H. Low, L. P. Stubbs, E. Drent in A
Catalyst for the Carbonylation of Alkenes. Pantent WO2017135897,
2017.
T. J. Korstanje, J. I. van der Vlugt, C. J. Elsevier, B. de Bruin, Science
2015, 350, 298-302.
[41] C. H. Low, J. D. Nobbs, M. van Meurs, L. P. Stubbs, E. Drent, S.
Aitipamula, M. H. L. Pung, Organometallics 2015, 34, 4281-4292.
[42] G. Verspui, J. Feiken, G. Papadogianakis, R. A. Sheldon, J. Mol. Catal.
A: Chem. 1999, 146, 299-307.
R. Russo, C. de Caro, C. Avagliano, C. Cristiano, G. la Rana, G. M.
Raso, R. B. Canani, R. Meli, A. Calignano, Pharmacol. Res. 2016, 103,
279-291.
[9]
A. E. Kerenkan, F. Béland, T.-O. Do, Catal. Sci. Technol. 2016, 6, 971-
987.
[43] I. del Rıo, N. Ruiz, C. Claver, L. A. van der Veen, P. W. N. M. van
́
Leeuwen, J. Mol. Catal. A: Chem. 2000, 161, 39-48.
[44] I. del Río, C. Claver, P. W. N. M. van Leeuwen, Eur. J. Inorg. Chem.
2001, 2719-2738.
[10] W. Liu, T. Liu, T. Liu, T. Liu, J. Xin, W. C. Hiscox, H. Liu, L. Liu, J.
Zhang, Ind. Eng. Chem. Res. 2017, 56, 3920-3927.
[11] E. Sharmin, F. Zafar, D. Akram, M. Alam, S. Ahmad, Ind. Crops Prod.
2015, 76, 215-229.
[45] C. T. Estorach, A. Orejón, N. Ruiz, A. M. Masdeau-Bultó, G. Laurenczy,
Eur. J. Inorg. Chem. 2006, 22, 2524-3531.
[12] H. Doucet. B. Martin-Vaca, C. Bruneau, P. H. Dixneuf, J. Org. Chem.
1995, 60, 7247-7255.
[46] A. Ionescu, G. Laurenczy, O. F. Wendt, Dalton Trans. 2006, 32, 3934-
3940.
[13] M. Jørgensen, S. Lee, X. Liu, J. P. Wolkowski, J. F. Hartwig, J. Am.
Chem. Soc. 2002, 124, 12557-12565.
[47] V. Goldach, L. Falivene, L. Caporaso, L. Cavallo, S. Mecking, ACS
Catal. 2016, 6, 8229-8238.
[14] Organic Market Organic Acids Market by Type, Application, Region –
2022. Report Code FB 4344, MarketsandMarkets, 2017.
[15] A. Brennführer, H. Neumann, M. Beller, ChemCatChem 2009, 1, 28-41.
[16] H. J. Arpe in Industrielle Organische Chemie: Bedeutende Vor- und
Zwischenprodukte, Wiley-VCH, Weinheim, 2007.
[48] F. Bertoux, S. Tilloy, E. Monflier, Y. Castanet, A. Mortreux, J. Mol. Catal.
A: Chem. 1999, 138, 53-57.
[49] K. Karlsson, A. Ionescu, C. Andersson, J. Mol. Catal. A: Chem. 2006,
259, 231-237.
[50] C. J. Moulton, B. L. Shaw, J. Chem. Soc., Chem. Commun. 1976, 365-
366.
[17] L. Vanoye, A. Aloui, M. Pablos, R. Philippe, A. Percheron, A. Favre-
Réguillon, de C. Bellefon, Org. Lett. 2013, 15, 5978-5981.
[18] R. W. Johnson, E. Fritz in Fatty Acids in Industry: Properties,
Derivatives, Applications, Marcel Dekker Inc., 1989.
[51] E. Drent, R. Erenst, W. W. Jager, C. A. Krom, T. M. Nisbet, J. A. M. van
Broekhoven in Process for the Preparation of Adipic Acid from N-
Pentenoic Acid. Pantent WO2006125801, 2006.
[19] F. D. Gunstone in Fatty Acid and Lipid Chemistry, Springer, Dordrecht,
1996.
[52] J. D. Nobbs, N. Z. B. Zainal, J. Tan, E. Drent, L. P. Stubbs, C. Li, ꢀ S. C.
Y. Lim, D. G. A. Kumbang, M. van Meurs, ChemistrySelect 2016, 3,
539-544.
[20] V. Y. Shtern in The Gas-Phase Oxidation of Hydrocarbons (Ed. B. P.
Mullins) Pergamon, Oxford, 1964.
[53] C. Amatore, A. Jutand, M. A. M'Barki, Organometallics 1992, 11, 3009-
3013.
[21] B. Cornils, W. A. Herrmann, M. Beller, R. Paciello in Applied
Homogeneous Catalysis with Organometallic Compounds:
A
[54] C. Amatore, E. Carre, A. Jutand, M. A. M'Barki, Organometallics 1995,
14, 1818-1826.
Comprehensive Handbook in Three Volumes, Wiley‐VCH, Weinheim,
2017.
[55] K. Dong, X. Fang, S. Gülak, R. Franke, A. Spannenberg, H. Neumann,
R.Jackstell, M. Beller, Nat. Commun. 2017, 8, 14117-14123.
[56] K. Dong, R. Sang, Z. Wei, J. Liu, R. Dühren, A. Spannenberg, H. Jiao,
H. Neumann, R. Jackstell, R. Franke, M. Beller, Chem. Sci. 2018, 9,
2510-2516.
[22] W. Reppe, H. Kröper, Liebigs Ann. Chem. 1953, 582, 38-71.
[23] W. Reppe, H. Kröper, N. von Kutepow, H. J. Pistor, Liebigs Ann. Chem.
1953, 582, 72-86.
[24] W. Reppe, H. Kröper, H. J. Pistor, O. Weissbarth, Liebigs Ann. Chem.
1953, 582, 87-116.
[57] K. Dong, R. Sang, X. Fang, R. Franke, A. Spannenberg, H. Neumann,
R. Jackstell, M. Beller, Angew. Chem., Int. Ed. 2017, 56, 5267−5271.
[58] R. Sang, P. Kucmierczyk, K. Dong, R. Frank, H. Neumann, R. Jackstell,
M. Beller, J. Am. Chem. Soc. 2018, 140, 5217-5223.
[59] B. Haven in Global and Chinese Isononanoic Acid Industry Market
Research Report 2018, Radiant Insight, San Francisco, 2018.
[60] J. Kubitschke, H. Lange, H. Strutz in Carboxylic Acids, Aliphatic.
Ullmann's Encyclopedia of Industrial Chemistry, Wiley‐VCH, Weinheim,
2014.
[25] W.Reppe, H. Vetter, Liebigs Ann. Chem. 1953, 582, 133-161.
[26] N. von Kutepow, K. Bittler, D. Neubauer in Carbonylation of Olefinically
Unsaturated Compounds. Pantent US3437676A, 1969.
[27] D. M. Fenton, J. Org. Chem. 1973, 38, 3192-3198.
[28] H. Alper, N. Hamel, J. Am. Chem. Soc. 1990, 112, 2803-2804.
[29] J.-Y. Yoon, E. J. Jang, K. H. Lee, J. S. Lee, J. Mol. Catal. A: Chem.
1997, 118, 181-187.
[30] S. Jayasree, A. Seayad, R. V. Chaudhari, Org. Lett. 2000, 2, 203-206.
[31] A. Seayad, S. Jayasree, R. V. Chaudhari, Catal. Lett. 1999, 61, 99-103.
[32] H. Alper, J. B. Woell, B. Despeyroux, D. J. H. Smith, J. Chem. Soc.,
Chem. Commun. 1983, 0, 1270-1271.
[61] J. Dai, W. Ren, H. Wang, Y. A. Shi, Org. Biomol. Chem. 2015, 13,
8429−8432.
[62] J. C. Rodriguez, D. F. Foster, G. R. Eastham, D. J. Cole-Hamilton,
Chem. Commun. 2004, 1720–1721.
[33] E. Drent in Process for the carbonylation of olefinically unsaturated
compounds with a palladium catalyst. Pantent EP0106379, 1984.
[63] A. A. N. M. Magro, L.-M. Robb, P. J. Pogorzelec, A. M. Z. Slawin, G. R.
Eastham, D. J. Cole-Hamilton, Chem. Sci. 2010, 1, 723-730.
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