Citation: Ren Lanhui, Gao Shuang. Recent Advances of the Oxidation of C—H Bonds to Ketones[J]. Chinese Journal of Organic Chemistry, ;2017, 37(6): 1338-1351. doi: 10.6023/cjoc201702022 shu

Recent Advances of the Oxidation of C—H Bonds to Ketones

  • Corresponding author: Gao Shuang, sgao@dicp.ac.cn
  • Received Date: 17 February 2017
    Revised Date: 6 April 2017

    Fund Project: the National Natural Science Foundation of China 21273225

Figures(17)

  • The ketones are important intermediates for the synthesis of fine chemicals, such as pharmaceuticals, natural products, agricultural chemicals, dyes, etc. The oxidation of C—H bonds is one of the most direct and efficient synthetic methods for the preparation of ketones. In this review, the oxidation of C—H bonds to ketones is reviewed.
  • 加载中
    1. [1]

      Simandil, T. Catalytic Activation of Dioxygen by Metal Complexes, Kluwer Aeademie Publishers, Dordrecht, 1992, 1.

    2. [2]

      Suresh, A. K.; Sharmat, M. M.; Sridhar, T. Ind. Eng. Chem. Res. 2000, 39, 3958.  doi: 10.1021/ie0002733

    3. [3]

      Ertl, G.; Knozinger, H.; Weitkam, P. J. Handbook of Heterogeneous Catalysis, Wiley & Sons-VCH Publishers, Weinheim, 1997.

    4. [4]

      Wang, L. H.; Li, H. Q.; Ke, M.; Zhao, S. Q.; Fan, Z. M. Nat. Gas Chem. Ind. 2001, 16, 53.  doi: 10.3969/j.issn.1007-3426.2001.02.001

    5. [5]

      Bernaard, M. Chem. Rev. 1992, 92, 1411.  doi: 10.1021/cr00014a008

    6. [6]

      Dolphin, D.; Traylor, T. G.; Xie, L. Y. Acc. Chem. Res. 1997, 30, 251.  doi: 10.1021/ar960126u

    7. [7]

      Lu, P.; Feng, C.; Luo, D. P. Acta Chim. Sinica 2015, 73, 1315.  doi: 10.3866/PKU.WHXB201504222

    8. [8]

      Chen, C.; Qiu, H. H. Chin. J. Org. Chem. 2016, 36, 826.
       

    9. [9]

      Xu, X.; Guan, Y. H.; Xu, D. C.; Li, X. S. Chin. J. Org. Chem. 2016, 36, 850.
       

    10. [10]

      Hu, Z. Y.; Tong, X. F.; Liu, G. X. Chin. J. Org. Chem. 2015, 35, 539.
       

    11. [11]

      Lu, Q. Q.; Yi, H.; Lei, A. W. Acta Chim. Sinica 2015, 73, 1245.  doi: 10.3969/j.issn.0253-2409.2015.10.013

    12. [12]

      Shilov, A. E.; Shulpin, G. B. Chem. Rev. 1997, 97, 2879.  doi: 10.1021/cr9411886

    13. [13]

      Crabtree, R. H. J. Organomet. Chem. 2004, 689, 4083.  doi: 10.1016/j.jorganchem.2004.07.034

    14. [14]

      Giri, R.; Shi, B. R.; Engle, K. M.; Maugel, N.; Yu, J. Q. Chem. Soc. Rev. 2009, 38, 3242.  doi: 10.1039/b816707a

    15. [15]

      Dick, A. R.; Sanford, M. S. Tetrahedron 2006, 62, 2439.  doi: 10.1016/j.tet.2005.11.027

    16. [16]

      Kleemann, A.; Engel, J.; Kutscher, B.; Reichert, D. Pharmaceutical Substances: Syntheses, Patents, Applications, 4th ed., Georg Thieme, Stuttgart, 2001.

    17. [17]

      Reis, D. C.; Pinto, M. C. X.; Souza-Fagundes, E. M.; Wardell, S. M. S. V.; Wardell, J. L.; Beraldo, H. Eur. J. Med. Chem. 2010, 45, 3904.  doi: 10.1016/j.ejmech.2010.05.044

    18. [18]

      Guyton, A. C.; Hall, J. E. Textbook of Medical Physiology, 11th ed., Philadelphia, PA, Elsevier Saunders, 2005.

    19. [19]

      Easmon, J.; Heinisch, G.; Pürstinger, G.; Langer, T.; Österreicher, J. K. J. Med. Chem. 1997, 40, 4420.  doi: 10.1021/jm970255w

    20. [20]

      Crook, K. E.; Mcelval, S. M.; Mceivain, S. M. J. Am. Chem. Soc. 1930, 52, 4006.  doi: 10.1021/ja01373a035

    21. [21]

      Huntress, E. H.; Walter, H. C. J. Am. Chem. Soc. 1948, 70, 3702.  doi: 10.1021/ja01191a046

    22. [22]

      Watson, P. L. J. Am. Chem. Soc. 1983, 21, 6491.

    23. [23]

      Barton, D. H. R.; Taylor, D. K.; Hu, B. Tretrahetron Lett. 1996, 8, 1133.

    24. [24]

      Fridovich, I. Science 1978, 201, 875.  doi: 10.1126/science.210504

    25. [25]

      Han, S.; Eltis, L. D.; Timmis, K. N.; Muchmore, S. W.; Bolin, J. T. Science 1995, 270, 976.  doi: 10.1126/science.270.5238.976

    26. [26]

      Ford, P. C.; Fernandez, B. O.; Lim, M. D. Chem. Rev. 2005, 105, 2439.  doi: 10.1021/cr0307289

    27. [27]

      Barton, D. H. R.; Doller, D. Acc. Chem. Res. 1992, 25, 504.  doi: 10.1021/ar00023a004

    28. [28]

      Barton, D. H. R. Chem. Soc. Rev. 1996, 25, 237.  doi: 10.1039/cs9962500237

    29. [29]

      Stavropoulos, P.; C-Elenligil-C-Etin, R.; Tapper, A. E. Acc. Chem. Res. 2001, 34, 745.  doi: 10.1021/ar000100+

    30. [30]

      Perkins, M. J. Chem. Soc. Rev. 1996, 25, 229.  doi: 10.1039/cs9962500229

    31. [31]

      Li, S. J.; Wang, Y. G. A. Tetrahedron Lett. 2005, 46, 8013.  doi: 10.1016/j.tetlet.2005.09.055

    32. [32]

      Chen, M. S.; White, M. C. Science 2010, 327, 566.  doi: 10.1126/science.1183602

    33. [33]

      Pieber, B.; Kappe, C. O. Green Chem. 2013, 15, 320.  doi: 10.1039/c2gc36896j

    34. [34]

      Szabó, F.; Pethó, B.; Gonda, Z.; Novák, Z. RSC Adv. 2013, 3, 4903.  doi: 10.1039/c3ra22856h

    35. [35]

      Napoly, F.; Kieffer, R.; Gérard, L. J.; Henry, C. G.; Draye, M.; Andrioletti, B. Tetrahedron Lett. 2015, 56, 2517.  doi: 10.1016/j.tetlet.2015.03.115

    36. [36]

      Fan, S.; Luan, Y. Wang, J. J.; Gao, H. Y.; Zhang, X. W.; Wang, G. J. Mol. Catal. A: Chem. 2015, 404~405, 186.

    37. [37]

      Al-Hunaiti, A.; Raisanen, M.; Repo, T. Chem. Commun. 2016, 52, 2043.  doi: 10.1039/C5CC07597A

    38. [38]

      Muhldorf, B.; Wolf, R. Angew. Chem., Int. Ed. 2016, 55, 427.  doi: 10.1002/anie.201507170

    39. [39]

      Komiya, N.; Naota, T.; Murahashi, S. I. Tetrahedron Lett. 1996, 37, 1633.  doi: 10.1016/0040-4039(96)00074-3

    40. [40]

      Velusamy, S.; Punniyamurthy, T. Tetrahedron Lett. 2003, 44, 8955.  doi: 10.1016/j.tetlet.2003.10.016

    41. [41]

      Wu, X. H.; Gorden, A. E. V. Eur. J. Org. Chem. 2009, 503.

    42. [42]

      Li, Y. C.; Lee, T. B.; Wang, T. Y.; Gamble, A. V. Gorden, A. E. V. J. Org. Chem. 2012, 77, 4628.  doi: 10.1021/jo300372q

    43. [43]

      Houwer, J. D.; Tehrani, K. A.; Maes, B. U. W. Angew. Chem., Int. Ed. 2012, 51, 2745.  doi: 10.1002/anie.201108540

    44. [44]

      Song, G. Q.; Lu, Y. X.; Zhang, Q.; Wang, F.; Ma, X. K.; Huang, X. F.; Zhang, Z. H. RSC Adv. 2014, 4, 30221.  doi: 10.1039/C4RA04076G

    45. [45]

      Ang, W. J.; Lam, Y. L. Org. Biomol. Chem. 2015, 13, 1048.  doi: 10.1039/C4OB02017K

    46. [46]

      Liu, J. M.; Zhang, X.; Yi H.; Liu, C.; Liu, R.; Zhang, H.; Zhuo, K. L.; Lei, A. W. C. Angew. Chem., Int. Ed. 2015, 54, 1261.  doi: 10.1002/anie.201409580

    47. [47]

      Lau, T. C.; Mak, C. K. Chem. Commun. 1995, 943.

    48. [48]

      Che, C. M.; Cheng, K. W.; Chan, M. C. W.; Lau, T. C.; Mak, C. K. J. Org. Chem. 2000, 65, 7996.  doi: 10.1021/jo0010126

    49. [49]

      Yi, C. S.; Kwon, K. H.; Lee, D. W. Org. Lett. 2009, 11, 1567.  doi: 10.1021/ol900097y

    50. [50]

      Yusubov, M. S.; Zagulyaeva, A. A.; Zhdankin, V. V. Chem. Eur. J. 2009, 15, 11091.  doi: 10.1002/(ISSN)1521-3765

    51. [51]

      Kojima, M.; Oisaki, K.; Kanai, M. Tetrahedron Lett. 2014, 55, 4736.  doi: 10.1016/j.tetlet.2014.06.038

    52. [52]

      Dai, W. Li, J.; Li, G. S.; Yang, H.; Wang, L. Y.; Gao, S. Org. Lett. 2013, 15, 4138.  doi: 10.1021/ol401812h

    53. [53]

      Dai, W.; Shang, S. S.; Chen, B.; Li, s.; Wang, L. Y.; Ren, L. H.; Gao, S. J. Org. Chem. 2014, 79, 6688.  doi: 10.1021/jo501178k

    54. [54]

      Dai, W.; Li, G. S.; Chen, B.; Wang, L. Y.; Gao, S. Org. Lett. 2015, 17, 904.  doi: 10.1021/acs.orglett.5b00018

    55. [55]

      Dai, W.; Li, J.; Chen, B.; Li, G. S.; Lv, Y.; Wang, L. Y.; Gao, S. Org. Lett. 2013, 15, 5658.  doi: 10.1021/ol402612x

    56. [56]

      Dai, W.; Li, G. S.; Wang, L. Y.; Chen, B.; Shang, S. S.; Lv, Y.; Gao, S. RSC Adv. 2014, 4, 46545.  doi: 10.1039/C4RA09832C

    57. [57]

      Dai, W.; Mi, Y.; Lv, Y.; Chen, B.; Li, G. S.; Chen, G. G.; Gao, S. Adv. Synth. Catal. 2016, 4, 667.

    58. [58]

      Dai, W.; Lv, Y.; Wang, L. Y.; Shang, S. S.; Chen, B.; Li, G. S.; Gao, S. Chem. Commun. 2015, 51, 11268.  doi: 10.1039/C5CC03657G

    59. [59]

      Lee, N. H.; Lee, C. S.; Jung, D. S. Tetrahedron Lett. 1998, 39, 1385.  doi: 10.1016/S0040-4039(98)00030-6

    60. [60]

      Pan, J. F.; Chen, K. J. Mol. Catal. A: Chem. 2001, 176, 19.  doi: 10.1016/S1381-1169(01)00238-2

    61. [61]

      Shing, T. K. M.; Yeung, Y. Y.; Su, P. L. Org. Lett. 2006, 8, 3149.  doi: 10.1021/ol0612298

    62. [62]

      Burange, A. S.; Kale, S. R.; Jayaram, R. V. Tetrahedron Lett. 2012, 53, 2989.  doi: 10.1016/j.tetlet.2012.03.091

    63. [63]

      Shen, D. Y.; Miao, C. X.; Wang, S. F. Xia, C. G.; Sun, W. Org. Lett. 2014, 16, 1108.  doi: 10.1021/ol4037083

    64. [64]

      Zou, C.; Zhao, M.; Wu, C. D. Catal. Commun. 2015, 66, 116.  doi: 10.1016/j.catcom.2015.03.031

    65. [65]

      Shaabani, A.; Hezarkhani, Z.; Badali, E. RSC Adv. 2015, 5, 61759.  doi: 10.1039/C5RA10522F

    66. [66]

      Ren, L. H.; Wang, L. Y.; Lv, Y.; Shang, S. S.; Bo Chen, B.; Gao, S. Green Chem. 2015, 17, 2369.  doi: 10.1039/C4GC02471K

    67. [67]

      Ren, L. H.; Wang, L. Y.; Lü, Y.; Li, G. S.; Gao, S. Chin. J. Catal. 2016, 37, 1216.

    68. [68]

      Ishii, Y.; Iwahama, T.; Sakaguchi, S.; Nakayama, K.; Nishiyama, Y. J. Org. Chem. 1996, 61, 4520.  doi: 10.1021/jo951970l

    69. [69]

      Minisci, F.; Punta, C.; Recupero, F.; Pedulli, F. F.; Franco, G. J. Org. Chem. 2002, 67, 2671.  doi: 10.1021/jo016398e

    70. [70]

      Shaabani, A.; Farhangi, E.; Rahmati, A. Appl. Catal. A-Gen. 2008, 338, 14.  doi: 10.1016/j.apcata.2007.12.014

    71. [71]

      Wang, J. Q.; He, L. N. New J. Chem. 2009, 33, 1637.  doi: 10.1039/b908993d

    72. [72]

      Chen, L.; Li, B. D.; Xu, Q. X.; Liu, D. B. Chin. Chem. Lett. 2013, 24, 849.

    73. [73]

      Islam, S. M.; Ghosh, K.; Molla, R. A.; Roy, S. A.; Salam, N.; Iqubal, M. A. J. Organomet. Chem. 2014, 774, 61.  doi: 10.1016/j.jorganchem.2014.10.010

    74. [74]

      Shaabani, A.; Keshipour, S.; Hamidzad, M.; Shaabani, S. J. Mol. Catal. A: Chem. 2014, 395, 494.  doi: 10.1016/j.molcata.2014.09.003

    75. [75]

      Hruszkewycz, D. P.; Miles, K. C.; Thielb, O. R.; Stahl, S. S. Chem. Sci. 2017, 8, 1282.  doi: 10.1039/C6SC03831J

    76. [76]

      Wu, X. F. Tetrahedron Lett. 2012, 53, 6123.  doi: 10.1016/j.tetlet.2012.08.149

    77. [77]

      Akhlaghinia, B.; Ebrahimabadi, H.; Goharshadi, E. K.; Samiee, S. Rezazadeh, S. J. Mol. Catal. A: Chem. 2012, 357, 67.  doi: 10.1016/j.molcata.2012.01.020

    78. [78]

      Pahari, S. K.; Pal, P.; Sinhamahapatra, A.; Saha, A.; Santra, C.; Ghosh, S. C.; Chowdhury, B.; Panda, A. B. RSC Adv. 2015, 5, 45144.  doi: 10.1039/C5RA05441A

    79. [79]

      Bien, S.; Segal, Y. J. Org. Chem. 1977, 42, 1685.  doi: 10.1021/jo00430a003

    80. [80]

      Noels, A. F.; Hubert, A. J.; Teyssie, P. J. Organomet. Chem. 1979, 166, 79.  doi: 10.1016/S0022-328X(00)91422-0

    81. [81]

      Moody, C. J.; Palmer, F. N. Tetrahedron Lett. 2001, 43, 139.

    82. [82]

      Doyle, M. P.; Westrum, L. J.; Wolthuis, W. N. E.; See, M. M.; Boone, W. P.; Bagheri, V.; Pearson, M. M. J. Am. Chem. Soc. 1993, 115, 958.  doi: 10.1021/ja00056a021

    83. [83]

      Doyle, M. P.; Ren, T. Chiral Dirhodium() Catalysts and Their Applications, Wiley, New York, 2001, 49, 113.

    84. [84]

      Das, K.; Kadish, K. M.; Bear, J. L. Inorg. Chem. 1978, 17, 930.  doi: 10.1021/ic50182a027

    85. [85]

      Zhu, T. P.; Ahsan, M. Q.; Malinski, T.; Kadish, K. M.; Bear, J. L. Inorg. Chem. 1984, 23, 2.  doi: 10.1021/ic00169a002

    86. [86]

      Catino, A. J.; Forslund, R. E.; Doyle, M. P. J. Am. Chem. Soc. 2004, 126, 13622.  doi: 10.1021/ja045330o

    87. [87]

      Catino, A. J.; Nichols, J. M.; Choi, H.; Gottipamula, S.; Doyle, M. P. Org. Lett. 2005, 7, 5167.  doi: 10.1021/ol0520020

    88. [88]

      Abudureheman, W.; Xiarepati, T.; Lu, C. D. Eur. J. Org. Chem. 2012, 3088.

    89. [89]

      Wang, Y.; Kuang, Y.; Wang, Y. H. Chem. Commun. 2015, 51, 5852.  doi: 10.1039/C4CC10336J

    90. [90]

      Matano, Y.; Nomura, H. J. Am. Chem. Soc. 2001, 123, 6443.  doi: 10.1021/ja010584k

    91. [91]

      Firouzabadi, H.; Iranpoor, N.; Amani, K. Synth. Commun. 2004, 34, 3587.  doi: 10.1081/SCC-200031036

    92. [92]

      Salvador, J. A. R.; Silvestre, S. M. Tetrahedron Lett. 2005, 46, 2581.  doi: 10.1016/j.tetlet.2005.02.080

    93. [93]

      Banik, B. K.; Venkatraman, M. S.; Mukhopadhyay, C.; Becker, F. F. Tetrahedron Lett. 1998, 39, 7247.  doi: 10.1016/S0040-4039(98)01556-1

    94. [94]

      Bonvin, Y.; Callens, E.; Larrosa, I.; Henderson, D. A.; Oldham, J.; Burton, A. J.; Barrett, A. G. M. Org. Lett. 2005, 7, 4549.  doi: 10.1021/ol051765k

    95. [95]

      Hoffmann-Roder, A.; Krause, N. Org. Biomol. Chem. 2005, 3, 387.  doi: 10.1039/B416516K

    96. [96]

      Cinellu, M. A.; Minghetti, G.; Cocco, F.; Stoccoro, S.; Zucca, A.; Manassero, M. Angew. Chem., Int. Ed. 2005, 44, 6892.  doi: 10.1002/(ISSN)1521-3773

    97. [97]

      Hashmia, S. K.; Hutchings, G. J. Angew. Chem., Int. Ed. 2006, 45, 7896.  doi: 10.1002/(ISSN)1521-3773

    98. [98]

      Li, Z.; Brouwer, C.; He, C. Chem. Rev. 2008, 108, 3239.  doi: 10.1021/cr068434l

    99. [99]

      Yao, T.; Zhang, X.; Larock, R. C. J. Am. Chem. Soc. 2004, 126, 11164.  doi: 10.1021/ja0466964

    100. [100]

      Sherry, B. D.; Toste, F. D. J. Am. Chem. Soc. 2004, 126, 15978.  doi: 10.1021/ja044602k

    101. [101]

      Wei, C.; Li, C. J. J. Am. Chem. Soc. 2003, 125, 9584.  doi: 10.1021/ja0359299

    102. [102]

      Zhang, L.; Kozmin, S. A. J. Am. Chem. Soc. 2004, 126, 11806.  doi: 10.1021/ja046112y

    103. [103]

      Yao, X.; Li, C. J. J. Am. Chem. Soc. 2004, 126, 6884.  doi: 10.1021/ja0482637

    104. [104]

      Teles, J. H.; Brode, S. Chabanas, M. Angew. Chem., Int. Ed. 1998, 37, 1415.  doi: 10.1002/(ISSN)1521-3773

    105. [105]

      Arcadi, A.; Giuseppe, S. D.; Marinelli, F.; Rossi E. Adv. Synth. Catal. 2001, 343, 443.  doi: 10.1002/(ISSN)1615-4169

    106. [106]

      Shi, X.; Gorin, D. J.; Tosite, F. D. J. Am. Chem. Soc. 2005, 127, 5802.  doi: 10.1021/ja051689g

    107. [107]

      Zhang, L.; Kozmin, S. A. J. Am. Chem. Soc. 2005, 127, 6962.  doi: 10.1021/ja051110e

    108. [108]

      Mamane, V.; Gress, T.; Krause, H.; Furstner, A. J. Am. Chem. Soc. 2004, 126, 8654.  doi: 10.1021/ja048094q

    109. [109]

      Luzung, M. R.; Markham, J. P.; Toste, F. D. J. Am. Chem. Soc. 2004, 126, 10858.  doi: 10.1021/ja046248w

    110. [110]

      Yang, C. G.; He, C. J. Am. Chem. Soc. 2005, 127, 6966.  doi: 10.1021/ja050392f

    111. [111]

      Shapiro, N. D.; Toste, F. D. J. Am. Chem. Soc. 2007, 129, 4160.  doi: 10.1021/ja070789e

    112. [112]

      Li, H. R.; Li, Z. P.; Shi, Z. J. Tetrahedron 2009, 65, 1856.  doi: 10.1016/j.tet.2008.12.055

    113. [113]

      Kühn, F. E.; Santos, A. M.; Gonçalves, I. S.; Romão, C. C.; Lopes, A. D. Appl. Organomet. Chem. 2001, 15, 43.  doi: 10.1002/(ISSN)1099-0739

    114. [114]

      Ghorai, P.; Dussault, P. H. Org. Lett. 2009, 11, 213.  doi: 10.1021/ol8023874

    115. [115]

      Ghorai, P.; Dussault, P. H. Org. Lett. 2008, 10, 4577.  doi: 10.1021/ol801859c

    116. [116]

      Bernini, R.; Mincione, E.; Barontini, M.; Fabrizi, G.; Pasqualetti, M.; Tempesta, S. Tetrahedron 2006, 62, 7733.  doi: 10.1016/j.tet.2006.05.069

    117. [117]

      Peng, H.; Lin, A.; Zhang, Y.; Jiang, H. L.; Zhou, J. C.; Cheng, Y. X.; Zhu, C. J.; Hu, H. W. ACS Catal. 2012, 2, 163.  doi: 10.1021/cs2003577

    118. [118]

      Yu, J. Q.; Corey, E. J. Org. Lett. 2002, 4, 2727.  doi: 10.1021/ol0262340

    119. [119]

      Urgoitia, G.; SanMartin, R.; Herrero, M. T.; Domínguez, E. Green Chem. 2011, 13, 2161.  doi: 10.1039/c1gc15390k

    120. [120]

      Anand, N.; Reddy, K. H. P.; Prasad, G. V. S.; Rao, K. S. R.; Burri, D. R. Catal. Commun. 2012, 23, 5.  doi: 10.1016/j.catcom.2012.02.023

    121. [121]

      Dohi, T.; Takenaga, N.; Takenaga, G. A.; Fujioka, H.; Kita, Y. J. Org. Chem. 2008, 73, 7365.  doi: 10.1021/jo8012435

    122. [122]

      Moriyama, K.; Takemura, M.; Togo, H. Org. Lett. 2012, 14, 2414.  doi: 10.1021/ol300853z

    123. [123]

      Kawabata, H.; Hayashi, M. Tetrahedron Lett. 2004, 45, 5457.  doi: 10.1016/j.tetlet.2004.05.030

    124. [124]

      Zhang, J. T.; Wang, Z. T.; Wang, Y.; Wan, C. F.; Zheng, X. Q.; Wang, Z. Y. Green Chem. 2009, 11, 1973.  doi: 10.1039/b919346b

    125. [125]

      Gao, Y. J.; Hu, G.; Zhong, J.; Shi, Z. J.; Zhu, Y. S.; Su, D. S.; Wang, J. G.; Bao, X. H.; Ma, D. Angew. Chem., Int. Ed. 2013, 52, 2109.  doi: 10.1002/anie.v52.7

    126. [126]

      Zhang, Z. G.; Gao, Y.; Liu, Y.; Li, J. J.; Xie, H. X.; Li, H.; Wang, W. Org. Lett. 2015, 17, 5492.  doi: 10.1021/acs.orglett.5b02877

    127. [127]

      Ma, J. Q.; Hu, Z. M.; Li, M. C.; Zhao, W. J.; Hua, X. Q.; Mo, W. M.; Hua, B. X.; Sun, N.; Shen, Z. L. Tetrahedron 2015, 71, 6733.  doi: 10.1016/j.tet.2015.07.042

    128. [128]

      Ren, L. H.; Wang, L. Y.; Lü, Y.; Li, G. S.; Gao, S. Org. Lett. 2015, 17, 2078.  doi: 10.1021/acs.orglett.5b00602

    129. [129]

      Yi, H.; Bian, C. L.; Hu, X.; Niua, L. B.; Lei, A. W. Chem. Commun. 2015, 51, 14046.  doi: 10.1039/C5CC06015J

    130. [130]

      Shaabani, A.; Laeini, M. S.; Shaabani, S.; Seyyedhamzeh, M. New J. Chem. 2016, 40, 2079.  doi: 10.1039/C5NJ02215K

  • 加载中
    1. [1]

      Peng YUELiyao SHIJinglei CUIHuirong ZHANGYanxia GUO . Effects of Ce and Mn promoters on the selective oxidation of ammonia over V2O5/TiO2 catalyst. Chinese Journal of Inorganic Chemistry, 2025, 41(2): 293-307. doi: 10.11862/CJIC.20240210

    2. [2]

      Peiyu Zhang Aixin Song Jingcheng Hao Jiwei Cui . 高频超声法制备聚多巴胺薄膜综合实验. University Chemistry, 2025, 40(6): 210-214. doi: 10.12461/PKU.DXHX202407081

    3. [3]

      Lihui Jiang Wanrong Dong Hua Yang Yongqing Xia Hongjian Peng Jun Yuan Xiaoqian Hu Zihan Zeng Yingping Zou Yiming Luo . Study on Extraction of p-Hydroxyacetophenone. University Chemistry, 2024, 39(11): 259-268. doi: 10.12461/PKU.DXHX202402056

    4. [4]

      Yue Zhao Yanfei Li Tao Xiong . Copper Hydride-Catalyzed Nucleophilic Additions of Unsaturated Hydrocarbons to Aldehydes and Ketones. University Chemistry, 2024, 39(4): 280-285. doi: 10.3866/PKU.DXHX202309001

    5. [5]

      Liangzhen Hu Li Ni Ziyi Liu Xiaohui Zhang Bo Qin Yan Xiong . A Green Chemistry Experiment on Electrochemical Synthesis of Benzophenone. University Chemistry, 2024, 39(6): 350-356. doi: 10.3866/PKU.DXHX202312001

    6. [6]

      Guojie Xu Fang Yu Yunxia Wang Meng Sun . Introduction to Metal-Catalyzed β-Carbon Elimination Reaction of Cyclopropenones. University Chemistry, 2024, 39(8): 169-173. doi: 10.3866/PKU.DXHX202401060

    7. [7]

      Danqing Wu Jiajun Liu Tianyu Li Dazhen Xu Zhiwei Miao . Research Progress on the Simultaneous Construction of C—O and C—X Bonds via 1,2-Difunctionalization of Olefins through Radical Pathways. University Chemistry, 2024, 39(11): 146-157. doi: 10.12461/PKU.DXHX202403087

    8. [8]

      Yongqing Kuang Jie Liu Jianjun Feng Wen Yang Shuanglian Cai Ling Shi . Experimental Design for the Two-Step Synthesis of Paracetamol from 4-Hydroxyacetophenone. University Chemistry, 2024, 39(8): 331-337. doi: 10.12461/PKU.DXHX202403012

    9. [9]

      Qiang HUZhiqi CHENZhong CHENXu WANGWeina WU . Pyridinium-chalcone-based ClO- fluorescent probe: Preparation and biological imaging applications. Chinese Journal of Inorganic Chemistry, 2025, 41(9): 1789-1795. doi: 10.11862/CJIC.20250086

    10. [10]

      Lu ZhuoranLi ShengkaiLu YuxuanWang ShuangyinZou Yuqin . Cleavage of C―C Bonds for Biomass Upgrading on Transition Metal Electrocatalysts. Acta Physico-Chimica Sinica, 2024, 40(4): 2306003-0. doi: 10.3866/PKU.WHXB202306003

    11. [11]

      Shuai TangZian WangMengyi ZhuXinyun ZhaoXiaoyun HuHua Zhang . Synthesis of organoboron compounds via heterogeneous C–H and C–X borylation. Chinese Chemical Letters, 2025, 36(5): 110503-. doi: 10.1016/j.cclet.2024.110503

    12. [12]

      Yurong Tang Yunren Shi Yi Xu Bo Qin Yanqin Xu Yunfei Cai . Innovative Experiment and Course Transformation Practice of Visible-Light-Mediated Photocatalytic Synthesis of Isoquinolinone. University Chemistry, 2024, 39(5): 296-306. doi: 10.3866/PKU.DXHX202311087

    13. [13]

      Zhuoming Liang Ming Chen Zhiwen Zheng Kai Chen . Multidimensional Studies on Ketone-Enol Tautomerism of 1,3-Diketones By 1H NMR. University Chemistry, 2024, 39(7): 361-367. doi: 10.3866/PKU.DXHX202311029

    14. [14]

      Yi YangXin ZhouMiaoli GuBei ChengZhen WuJianjun Zhang . Femtosecond transient absorption spectroscopy investigation on ultrafast electron transfer in S-scheme ZnO/CdIn2S4 photocatalyst for H2O2 production and benzylamine oxidation. Acta Physico-Chimica Sinica, 2025, 41(6): 100064-0. doi: 10.1016/j.actphy.2025.100064

    15. [15]

      Xin LiJia-Min LuBo LiChen ZhaoBei-Bei YangLi Li . Chiroptical sensing for remote chiral amines via a C–H activation reaction. Chinese Chemical Letters, 2025, 36(5): 110310-. doi: 10.1016/j.cclet.2024.110310

    16. [16]

      Tong LiLeping PanYan ZhangJihu SuKai LiKuiliang LiHu ChenQi SunZhiyong Wang . Electrochemical construction of 2,5-diaryloxazoles via N–H and C(sp3)-H functionalization. Chinese Chemical Letters, 2024, 35(4): 108897-. doi: 10.1016/j.cclet.2023.108897

    17. [17]

      Yi LuoLin Dong . Multicomponent remote C(sp2)-H bond addition by Ru catalysis: An efficient access to the alkylarylation of 2H-imidazoles. Chinese Chemical Letters, 2024, 35(10): 109648-. doi: 10.1016/j.cclet.2024.109648

    18. [18]

      Ke-Ai Zhou Lian Huang Xing-Ping Fu Li-Ling Zhang Yu-Ling Wang Qing-Yan Liu . Fluorinated metal-organic framework for methane purification from a ternary CH4/C2H6/C3H8 mixture. Chinese Journal of Structural Chemistry, 2023, 42(11): 100172-100172. doi: 10.1016/j.cjsc.2023.100172

    19. [19]

      Jialin HuangLiying FuZhanyong TangXiaoqiang MaXingda ZhaoDepeng Zhao . Cross-coupling of trifluoromethylarenes with alkynes C(sp)-H bonds and azoles C(sp2)-H bonds via photoredox/copper dual catalysis. Chinese Chemical Letters, 2025, 36(7): 110505-. doi: 10.1016/j.cclet.2024.110505

    20. [20]

      Shulei HuYu ZhangXiong XieLuhan LiKaixian ChenHong LiuJiang Wang . Rh(Ⅲ)-catalyzed late-stage C-H alkenylation and macrolactamization for the synthesis of cyclic peptides with unique Trp(C7)-alkene crosslinks. Chinese Chemical Letters, 2024, 35(8): 109408-. doi: 10.1016/j.cclet.2023.109408

Metrics
  • PDF Downloads(96)
  • Abstract views(6687)
  • HTML views(1170)

通讯作者: 陈斌, bchen63@163.com
  • 1. 

    沈阳化工大学材料科学与工程学院 沈阳 110142

  1. 本站搜索
  2. 百度学术搜索
  3. 万方数据库搜索
  4. CNKI搜索
Address:Zhongguancun North First Street 2,100190 Beijing, PR China Tel: +86-010-82449177-888
Powered By info@rhhz.net

/

DownLoad:  Full-Size Img  PowerPoint
Return