Corrigendum: Up the Hill: Selective Double-Bond Isomerization of Terminal 1,3-Dienes towards Z-1,3-Dienes or 2Z,4E-Dienes (Angewandte Chemie International Edition, (2012), 51, 5, (1270-1273), 10.1002/anie.201107512);Up the hill: Selective double-bond isomerization of terminal 1,3-dienes towards Z-1,3-dienes or 2Z,4E-dienes

Angewandte Chemie - International Edition

Volumn 51, Issue 5, 2012, Pages 1270-1273

  Pünner, Florian ^a   Schmidt, Anastasia ^a   Hilt, Gerhard ^a  

^a PHILIPPS UNIVERSITY MARBURG   (Germany)

Author keywords

cobalt; dienes; double bond migration; isomerization; stereoselectivity

Indexed keywords

CATALYSTS; COBALT; ISOMERIZATION; OLEFINS; STEREOSELECTIVITY;

1 ,3-DIENES; CATALYST PRECURSORS; CATALYZED REACTIONS; COBALT CATALYST SYSTEM; DIENES; DOUBLE BOND MIGRATION; DOUBLE-BOND ISOMERIZATION; SELECTIVE ISOMERIZATION;

ISOMERS;

EID: 84856200181     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201902504     Document Type: Erratum

References (59)

1. R. C. Larock, Comprehensive Organic Transformations, 2 nd ed., Wiley-VCH, 1999. For the synthesis of 1,3-dienes, see
2. R. Shintani, W.-L. Duan, S. Park, T. Hayashi, Chem. Commun. 2006, 3646
3. H. Yasui, H. Yorimitsu, K. Oshima, Synlett 2006, 1783
4. F. Tellier, C. Descoins, R. Sauvêtre, Tetrahedron 1991, 47, 7767
5. M. H. P. J. Aerssens, R. Van der Heiden, M. Heus, L. Brandsma, Synth. Commun. 1990, 20, 3421
6. W. Boland, N. Schroer, C. Sieler, M. Feigel, Helv. Chim. Acta 1987, 70, 1025.
7. Y. Kuriyama, Kokagaku 2003, 34, 205
8. H. Rau, Stud. Org. Chem. 1990, 40, 165
9. J. Saltiel, Y. P. Sun, Stud. Org. Chem. 1990, 40, 64.
10. W. Tsuzuki, Chem. Phys. Lipids 2010, 163, 741
11. C. Ferreri, M. Panagiotaki, C. Chatgilialoglu, Mol. Biotechnol. 2007, 37, 19.
12. D. Gauthier, A. T. Lindhardt, E. P. K. Olsen, J. Overgaard, T. Skrydstrup, J. Am. Chem. Soc. 2010, 132, 7998
13. G. Erdogan, D. B. Grotjahn, J. Am. Chem. Soc. 2009, 131, 10354
14. N. Catozzi, M. G. Edwards, S. A. Raw, P. Wasnaire, R. J. K. Taylor, J. Org. Chem. 2009, 74, 8343
15. T. J. Donohoe, T. J. C. O'Riordan, C. P. Rosa, Angew. Chem. 2009, 121, 1032
16. Angew. Chem. Int. Ed. 2009, 48, 1014
17. R. Uma, C. Crévisy, R. Grée, Chem. Rev. 2003, 103, 27
18. M. Mirza-Aghayan, R. Boukherroub, M. Bolourtchian, M. Hoseini, K. Tabar-Hydar, J. Organomet. Chem. 2003, 678, 1
19. I. R. Baxendale, A.-L. Lee, S. V. Ley, Synlett 2002, 516
20. M. Mayer, A. Welther, A. Jacobi von Wangelin, ChemCatChem 2011, 3, 1567.
21. F.-L. Wu, B. P. Ross, R. P. McGeary, Eur. J. Org. Chem. 2010, 1989
22. H. Firouzabadi, N. Iranpoor, M. Jafarpour, Tetrahedron Lett. 2005, 46, 4107
23. M. T. Reetz, M. Plachky, Synthesis 1976, 199.
24. M. A. Bohn, A. Schmidt, G. Hilt, M. Dindaroǧlu, H.-G. Schmalz, Angew. Chem. 2011, 123, 9863
25. Angew. Chem. Int. Ed. 2011, 50, 9689
26. G. Hilt, S. Roesner, Synthesis 2011, 662
27. M. Arndt, A. Reinhold, G. Hilt, J. Org. Chem. 2010, 75, 5203
28. G. Hilt, M. Danz, J. Treutwein, Org. Lett. 2009, 11, 3322
29. R. K. Sharma, T. V. RajanBabu, J. Am. Chem. Soc. 2010, 132, 3295
30. B. Saha, C. R. Smith, T. V. RajanBabu, J. Am. Chem. Soc. 2008, 130, 9000
31. M. Shirakura, M. Suginome, J. Am. Chem. Soc. 2008, 130, 5410
32. B. Saha, T. V. RajanBabu, J. Org. Chem. 2007, 72, 2357
33. N. Lassauque, G. Franciò, W. Leitner, Adv. Synth. Catal. 2009, 351, 3133
34. N. Lassauque, G. Franciò, W. Leitner, Eur. J. Org. Chem. 2009, 3199
35. M. M. P. Grutters, C. Müller, D. Vogt, J. Am. Chem. Soc. 2006, 128, 7414.
36. J. S. Yadav, M. Y. Valli, A. R. Prasad, Pure Appl. Chem. 2001, 73, 1157
37. M. Winter, F. Näf, A. Furrer, W. Pickenhagen, W. Giersch, A. Meister, B. Willhalm, W. Thommen, G. Ohloff, Helv. Chim. Acta 1979, 62, 135
38. R. Kaiser, Dev. Food Sci. 1988, 18, 669. See also
39. W. Boland, K. Jakoby, L. Jaenicke, Helv. Chim. Acta 1982, 65, 2355.
40. R. J. Ely, J. P. Morken, J. Am. Chem. Soc. 2010, 132, 2534.
41. A. Mostafavi, T. Shamspur, D. Afazali, S. M. Mirtadzadini, J. Essent. Oil Res. 2010, 22, 300
42. H.-L. Wang, G. P. Svensson, O. Rosenberg, M. Bengtsson, E. V. Jirle, C. Löfstedt, J. Chem. Ecol. 2010, 36, 305
43. L. Van Vang, M. Ishitani, F. Komai, M. Yamamoto, T. Ando, Appl. Entomol. Zool. 2006, 41, 507
44. L. Van Vang, S.-I. Inomata, M. Kinjo, F. Komai, T. Ando, J. Chem. Ecol. 2005, 31, 859
45. H. J. Bestmann, J. Süß, O. Vostrowsky, Liebigs Ann. Chem. 1981, 2117
46. H. J. Bestmann, J. Süß, O. Vostrowsky, Tetrahedron Lett. 1978, 19, 3329.
47. G. Erker, G. Kehr, R. Fröhlich, J. Organomet. Chem. 2005, 690, 6254.
48. S.-C. Zhao, X.-Z. Shu, K.-G. Ji, A.-X. Zhou, T. He, X.-Y. Liu, Y.-M. Liang, J. Org. Chem. 2011, 76, 1941
49. X.-Z. Shu, K.-G. Ji, S.-C. Zhao, Z.-J. Zheng, J. Chen, L. Lu, X.-Y. Liu, Y.-M. Liang, Chem. Eur. J. 2008, 14, 10556
50. Y. S. Park, S. C. Wang, D. J. Tantillo, R. D. Little, J. Org. Chem. 2007, 72, 4351
51. Y. Kubota, K. Satake, H. Okamoto, M. Kimura, Org. Lett. 2006, 8, 5469
52. I. V. Alabugin, M. Manoharan, B. Breiner, F. D. Lewis, J. Am. Chem. Soc. 2003, 125, 9329
53. B. A. Hess, Jr., J. E. Baldwin, J. Org. Chem. 2002, 67, 6025
54. M. J. Robins, Z. O. Guo, M. C. Samano, S. F. Wnuk, J. Am. Chem. Soc. 1999, 121, 1425
55. A. Kless, M. Nendel, S. Willsey, K. N. Houk, J. Am. Chem. Soc. 1999, 121, 4524
56. Y. Lin, E. Turos, J. Am. Chem. Soc. 1999, 121, 856
57. P. A. Parziale, J. A. Berson, J. Am. Chem. Soc. 1990, 112, 1650
58. K. Wu, M. M. Midland, W. H. Okamura, J. Org. Chem. 1990, 55, 4381
59. G. Y. Shen, R. Tapia, W. H. Okamura, J. Am. Chem. Soc. 1987, 109, 7499.