Synthetic applications of arylboronic acid via an aryl radical transfer pathway

Organic and Biomolecular Chemistry

Volumn 11, Issue 46, 2013, Pages 7999-8008

  Yan, Guobing ^a   Yang, Minghua ^a   Wu, Xiangmei ^a  

^a LISHUI UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ARYLBORONIC ACIDS; CARBON-BORON BONDS; CARBON-HETEROATOM BONDS; FUNCTIONALIZATIONS; MANGANESE ACETATE; ORGANOMETALLIC INTERMEDIATES; RADICAL PRECURSOR; SYNTHETIC APPLICATION;

ORGANOMETALLICS;

CARBON;

EID: 84887451063     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c3ob41851k     Document Type: Review

References (66)

1. J. Iqbal B. Bhatia N. K. Nayyar Chem. Rev. 1994 94 519 564
2. M. P. Sibi N. A. Porter Acc. Chem. Res. 1999 32 163 171
3. A. Gansäuer H. Bluhm Chem. Rev. 2000 100 2771 2788
4. J. Robertson J. Pillai R. K. Lush Chem. Soc. Rev. 2001 30 94 103
5. A. Studer Chem. Soc. Rev. 2004 33 263 271
6. S. S. Brown J. Stutz Chem. Soc. Rev. 2012 41 6405 6447
7. M. D. Tzirakis M. Orfanopoulos Chem. Rev. 2013 113 5262 5321
8. F. Dénès C. H. Schiesser P. Renaud Chem. Soc. Rev. 2013 42 7900 7942
9. W. R. Bowman J. M. D. Storey Chem. Soc. Rev. 2007 36 1803 1822
10. C. Galli Chem. Rev. 1988 88 765 792
11. M. R. Heinrich Chem.-Eur. J. 2009 15 820 833
12. F. Mo G. Dong Y. Zhang J. Wang Org. Biomol. Chem. 2013 11 1582 2593
13. D. P. Hari B. König Angew. Chem., Int. Ed. 2013 52 4734 4743
14. T. B. Patrick P. R. Willaredt D. J. DeGonia J. Org. Chem. 1985 50 2232 2235
15. V. V. Smalius V. M. Naidan Russ. J. Gen. Chem. 2006 76 1295 1298
16. T. Varea M. E. González-Núñez J. Rodrigo-Chiner G. Asensio Tetrahedron Lett. 1989 30 4709 4712
17. A. S. Demir Ö. Reis E. Özgül-Karaaslan J. Chem. Soc., Perkin Trans. 1 2001 3042 3045
18. A. S. Demir Ö. Reis M. Emrullahoglu Tetrahedron 2002 58 8055 8058
19. A. S. Demir H. Findik Tetrahedron 2008 64 6196 6201
20. T. Taniguchi H. Zaimoku H. Ishibashi Chem.-Eur. J. 2011 17 4307 4312
21. Z.-X. Chen G.-W. Wang J. Org. Chem. 2005 70 2380 2383
22. H. Jasch J. Scheumann M. R. Heinrich J. Org. Chem. 2012 77 10699 10706
23. S. E. Vaillard and A. Studer, Radical Arylations, in Encyclopedia of Radicals in Chemistry, Biology, and Materials, ed., C. Chatgilialoglu, and, A. Studer, Wiley, New York, 2012, vol. 2
24. H. Jasch and M. R. Heinrich, Tin Hydrides and Functional Group Transformations, in Encyclopedia of Radicals in Chemistry, Biology, and Materials, ed., C. Chatgilialoglu, and, A. Studer, Wiley, New York, 2012, vol. 2
25. G. Pratsch and M. R. Heinrich, in Topics in Current Chemistry, ed., M. R. Heinrich, and, A. Gansäuer, Springer, Weinheim, 2012, vol. 320, pp. 33-60
26. L. Wang G. Yan X. Zhang Chin. J. Org. Chem. 2012 32 1864 1871
27. A. Studer D. P. Curran Angew. Chem., Int. Ed. 2011 50 5018 5022
28. M. Goez G. Eckert U. Müller J. Phys. Chem. A 1999 103 5714 5721
29. Boronic Acids: Preparation and Applications in Organic Synthesis and Medicine, ed., D. G. Hall, Wiley-VCH, Weinheim, Germany, 2005
30. N. Miyaura A. Suzuki Chem. Rev. 1995 95 2457 2483
31. N. Miyaura Top. Curr. Chem. 2002 219 11 59
32. M. Mondal U. Bora RSC Adv. 2013 3 18716 18754
33. A. S. Demir Ö. Reis M. Emrullahoglu J. Org. Chem. 2003 68 578 580
34. A. S. Demir H. Findik Tetrahedron 2008 64 6196 6201
35. S. Demir H. Findik N. Saygili N. T. Subasi Tetrahedron 2010 66 1308 1312
36. S. K. Guchhait M. Kashyap S. Saraf Synthesis 2010 1166 1170
37. A. Dickschat A. Studer Org. Lett. 2010 12 3972 3974
38. M. Tobisu K. Koh T. Furukawa N. Chatani Angew. Chem., Int. Ed. 2012 51 11363 11366
39. G. Sorin R. M. Malloquin Y. Contie A. Baralle M. Malacria J.-P. Goddard L. Fensterbank Angew. Chem., Int. Ed. 2010 49 8721 8723
40. G. A. Molander V. Colombel V. A. Braz Org. Lett. 2011 13 1852 1855
41. U. Halbes-Letinois J.-M. Weibel P. Pale Chem. Soc. Rev. 2007 36 759 769
42. Y. Yamamoto Chem. Rev. 2008 108 3199 3222
43. M. Naodovic H. Yamamoto Chem. Rev. 2008 108 3132 3148
44. M. Álvarez-Corral M. Muñoz-Dorado I. Rodríguez- García Chem. Rev. 2008 108 3174 3198
45. Z. Li C. He Eur. J. Org. Chem. 2006 4313 4322
46. I. B. Seiple S. Su R. A. Rodriguez R. Gianatassio Y. Fujiwara A. L. Sobel P. S. Baran J. Am. Chem. Soc. 2010 132 13194 13196
47. Y. Fujiwara V. Domingo I. B. Seiple R. Gianatassio M. D. Bel P. S. Baran J. Am. Chem. Soc. 2011 133 3292 3295
48. J. W. Lockner D. D. Dixon R. Risgaard P. S. Baran Org. Lett. 2011 13 5628 5631
49. N. R. Patel R. A. Flowers II J. Am. Chem. Soc. 2013 135 4672 4675
50. C. Bolm J. Legros J. L. Paih L. Zani Chem. Rev. 2004 104 6217 6254
51. A. Correa O. G. Mancheno C. Bolm Chem. Soc. Rev. 2008 37 1108 1117
52. B. Sherry A. Fürstner Acc. Chem. Res. 2008 41 1500 1511
53. N. Uchiyama E. Shirakawa R. Nishikawa T. Hayashi Chem. Commun. 2011 47 11671 11673
54. J. Wang S. Wang G. Wang J. Zhang X.-Q. Yu Chem. Commun. 2012 48 11769 11771
55. C. Qin W. Zhou F. Chen Y. Ou N. Jiao Angew. Chem., Int. Ed. 2011 50 12595 12599
56. K. Komeyama T. Kashihara K. Takaki Tetrahedron Lett. 2013 54 1084 1086
57. P. P. Singh S. K. Aithagani M. Yadav V. P. Singh R. A. Vishwakarma J. Org. Chem. 2013 78 2639 2648
58. V. B. Phapale D. J. Cárdenas Chem. Soc. Rev. 2009 38 1598 1607
59. D.-G. Yu B.-J. Li Z.-J. Shi Acc. Chem. Res. 2010 43 1486 1495
60. B. M. Rosen K. W. Quasdorf D. A. Wilson N. Zhang A.-M. Resmerita N. K. Garg V. Percec Chem. Rev. 2011 111 1346 1416
61. R. Jana T. P. Pathak M. S. Sigman Chem. Rev. 2011 111 1417 1492
62. X. Hu Chem. Sci. 2011 2 1867 1886
63. F.-S. Han Chem. Soc. Rev. 2013 42 5270 5298
64. D. Liu C. Liu H. Li A. Lei Angew. Chem., Int. Ed. 2013 52 4453 4456
65. G. Yan M. Yang Org. Biomol. Chem. 2013 11 2554 2566
66. S. Manna S. Maity S. Rana S. Agasti D. Maiti Org. Lett. 2012 14 1736 1739