综述与进展

氢原子转移介导的烷烃C(sp3)—H选择性官能团化研究进展

  • 王淼 ,
  • 黄雅豪 ,
  • 胡鹏
展开
  • 中山大学化学学院 绿色化学与分子工程研究所 广东省高等学校功能分子工程基础研究卓越中心Lehn功能材料研究所 广州 510275

收稿日期: 2024-07-14

  修回日期: 2024-09-11

  网络出版日期: 2024-10-29

基金资助

广东省科技厅(2019QN01L151); 广东省科技厅(2023A0505050137); 广东省科技厅(2022A1515011215)

Recent Advances in Hydrogen Atom Transfer Induced Selective C(sp3)—H Functionalization of Alkanes

  • Miao Wang ,
  • Yahao Huang ,
  • Peng Hu
Expand
  • Lehn Institute of Functional Materials, Guangdong Basic Research Center of Excellence for Functional Molecular Engineering, Institute of Green Chemistry and Molecular Engineering, School of Chemistry, Sun Yat-sen University, Guangzhou 510275

Received date: 2024-07-14

  Revised date: 2024-09-11

  Online published: 2024-10-29

Supported by

Guangdong Provincial Science and Technology Department(2019QN01L151); Guangdong Provincial Science and Technology Department(2023A0505050137); Guangdong Provincial Science and Technology Department(2022A1515011215)

摘要

作为一种高度原子经济性和步骤经济性的策略, 通过烷烃C(sp3)—H键的官能团化, 直接将烷烃转化成附加值更高的化学品, 一直备受关注. 然而由于烷烃C(sp3)—H键广为人知的惰性, 控制非活化C(sp3)—H键官能团化的化学选择性和区域选择性是一项重大的挑战. 作为一种近期重新引起关注的方法, 相比以往过渡金属催化, 利用氢原子转移(HAT)实现C(sp3)—H键选择性官能团化有着其独特之处. 在此, 对最近兴起的各种HAT介导的非活化C(sp3)—H键官能团化的方法进行了分析, 按照官能团化的选择性分类, 重点介绍了目前实现区域选择性控制的方法. 最后总结了目前方法的局限性, 并对这一领域当前的挑战和未来的发展方向进行了展望.

本文引用格式

王淼 , 黄雅豪 , 胡鹏 . 氢原子转移介导的烷烃C(sp3)—H选择性官能团化研究进展[J]. 有机化学, 2025 , 45(2) : 477 -497 . DOI: 10.6023/cjoc202407027

Abstract

As a highly atom-economical and step-economic strategy, the functionalization of alkane C(sp3)—H bonds to directly convert alkanes into higher value-added chemicals has been a subject of great interest. However, due to the well-known inertness of alkane C(sp3)—H bonds, controlling the chemical selectivity and regioselectivity of non-activated C(sp3)—H bond functionalization poses a significant challenge. Recently, the utilization of hydrogen atom transfer (HAT) for achieving selectivity in C(sp3)—H bond functionalization has attracted renewed attention as a method distinct from traditional transition metal-catalyzed approaches. Herein, various HAT-mediated non-activated C(sp3)—H bond functionalization methods are analyzed based on selectivity of functionalization with a focus on methods that have achieved regioselectivity control. The current limitations of existing methods are summarized and the current challenges and future directions in this field are outlooked.

参考文献

[1]
Ward, J. M. Fuel Process. Technol. 1993, 35, 55.
[2]
Weitkamp, J. ChemCatChem 2012, 4, 292.
[3]
Wang, Y.; Hu, P.; Yang, J.; Zhu, Y.-A.; Chen, D. Chem. Soc. Rev. 2021, 50, 4299.
[4]
Khake, S. M.; Chatani, N. Trends Chem. 2019, 1, 524.
[5]
Gandeepan, P.; Müller, T.; Zell, D.; Cera, G.; Warratz, S.; Ackermann, L. Chem. Rev. 2018, 119, 2192.
[6]
Chu, J. C. K.; Rovis, T. Angew. Chem., Int. Ed. 2017, 57, 62.
[7]
Hartwig, J. F.; Larsen, M. A. ACS Cent. Sci. 2016, 2, 281.
[8]
He, J.; Wasa, M.; Chan, K. S. L.; Shao, Q.; Yu, J.-Q. Chem. Rev. 2016, 117, 8754.
[9]
Arndtsen, B. A.; Bergman, R. G.; Mobley, T. A.; Peterson, T. H. Acc. Chem. Res. 1995, 28, 154.
[10]
Davies, H. M. L.; Manning, J. R. Nature 2008, 451, 417.
[11]
Davies, H. M. L.; Morton, D. ACS Cent. Sci. 2017, 3, 936.
[12]
Mayer, J. M. Acc. Chem. Res. 2010, 44, 36.
[13]
Capaldo, L.; Ravelli, D.; Fagnoni, M. Chem. Rev. 2021, 122, 1875.
[14]
Chang, L.; Wang, S.; An, Q.; Liu, L. W.; Wang, H.; Li, Y.; Feng, K.; Zuo, Z. Chem. Sci. 2023, 14, 6841.
[15]
Huang, C.-Y.; Li, J.; Li, C.-J. Chem. Sci. 2022, 13, 5465.
[16]
Capaldo, L.; Ravelli, D. Eur. J. Org. Chem. 2017, 2017, 2056.
[17]
Sarkar, S.; Cheung, K. P. S.; Gevorgyan, V. Chem. Sci. 2020, 11, 12974.
[18]
Taniguchi, T. Synthesis 2017, 49, 3511.
[19]
Cheng, S.; Li, Q.; Cheng, X.; Lin, Y.; Gong, L. Chin. J. Chem. 2022, 40, 2825.
[20]
Roberts, B. P. Chem. Soc. Rev. 1999, 28, 25.
[21]
Salamone, M.; Bietti, M. Acc. Chem. Res. 2015, 48, 2895.
[22]
Ravelli, D.; Fagnoni, M.; Fukuyama, T.; Nishikawa, T.; Ryu, I. ACS Catal. 2017, 8, 701.
[23]
Galeotti, M.; Salamone, M.; Bietti, M. Chem. Soc. Rev. 2022, 51, 2171.
[24]
Matsumoto, A.; Maruoka, K. Asian J. Org. Chem. 2024, 13, e202300580.
[25]
Wang, Y.; Li, G.-X.; Yang, G.; He, G.; Chen, G. Chem. Sci. 2016, 7, 2679.
[26]
He, Q.; Cao, Z.; Zhang, Y.; Chen, G.; Wang, Y. Adv. Synth. Catal. 2023, 365, 2711.
[27]
Fawcett, A.; Keller, M. J.; Herrera, Z.; Hartwig, J. F. Angew. Chem., Int. Ed. 2021, 60, 8276.
[28]
Zhao, J.; Zhang, J.; Fang, P.; Wu, J.; Wang, F.; Liu, Z.-Q. Green Chem. 2024, 26, 507.
[29]
Kuang, Y.; Cao, H.; Tang, H.; Chew, J.; Chen, W.; Shi, X.; Wu, J. Chem. Sci. 2020, 11, 8912.
[30]
Mello, R.; Fiorentino, M.; Fusco, C.; Curci, R. J. Am. Chem. Soc. 1989, 111, 6749.
[31]
Sakaguchi, S.; Kato, S.; Iwahama, T.; Ishii, Y. Bull. Chem. Soc. Jpn. 1998, 71, 1237.
[32]
Kiyokawa, K.; Ito, R.; Takemoto, K.; Minakata, S. Chem. Commun. 2018, 54, 7609.
[33]
Paolillo, J. M.; Duke, A. D.; Gogarnoiu, E. S.; Wise, D. E.; Parasram, M. J. Am. Chem. Soc. 2023, 145, 2794.
[34]
Guo, S.; Zhang, X.; Tang, P. Angew. Chem., Int. Ed. 2015, 54, 4065.
[35]
Wu, H.; Xiao, Z.; Wu, J.; Guo, Y.; Xiao, J.-C.; Liu, C.; Chen, Q.-Y. Angew. Chem., Int. Ed. 2015, 54, 4070.
[36]
Zhao, Y.; Lin, J.-H.; Hang, X.-C.; Xiao, J.-C. J. Org. Chem. 2018, 83, 14120.
[37]
Mukherjee, S.; Maji, B.; Tlahuext-Aca, A.; Glorius, F. J. Am. Chem. Soc. 2016, 138, 16200.
[38]
Schirmer, T. E.; Rolka, A. B.; Karl, T. A.; Holzhausen, F.; K?nig, B. Org. Lett. 2021, 23, 5729.
[39]
Zhang, H.; Wang, Q.; Wang, Y.; Yuan, Z.; Gao, F.; Britton, R. Asian J. Org. Chem. 2021, 10, 2566.
[40]
Zhang, S.; Cao, S.; Lin, Y.-M.; Sha, L.; Lu, C.; Gong, L. Chin. J. Catal. 2022, 43, 564.
[41]
Antonchick, A. P.; Burgmann, L. Angew. Chem., Int. Ed. 2013, 52, 3267.
[42]
Fukuyama, T.; Nishikawa, T.; Yamada, K.; Ravelli, D.; Fagnoni, M.; Ryu, I. Org. Lett. 2017, 19, 6436.
[43]
Li, Y.; Lei, M.; Gong, L. Nat. Catal. 2019, 2, 1016.
[44]
Wang, M.; Zhang, Z.; Xiong, C.; Sun, P.; Zhou, C. ChemistrySelect 2022, 7, e202200816.
[45]
Wang, M.; Zhang, Y.; Yang, X.; Sun, P. Org. Biomol. Chem. 2022, 20, 2467.
[46]
Sheng, H.; Zhang, B.-B.; Liu, Q.; Yang, Z.-S.; Wang, Z.-X.; Chen, X.-Y. Sci. China: Chem. 2022, 65, 2494.
[47]
Li, Y.; Guo, S.-G.; Li, Q.; Zheng, K. Nat. Commun. 2023, 14, 6225.
[48]
Jha, R. K.; Rohilla, K.; Jain, S.; Parganiha, D.; Kumar, S. Chem.- Eur. J. 2024, 30, e202303537.
[49]
Zhang, X.; Yang, H.; Tang, P. Org. Lett. 2015, 17, 5828.
[50]
Day, C. S.; Fawcett, A.; Chatterjee, R.; Hartwig, J. F. J. Am. Chem. Soc. 2021, 143, 16184.
[51]
Ghosh, S. K.; Hu, M.; Comito, R. J. Chem.-Eur. J. 2021, 27, 17601.
[52]
Xia, J.-B.; Ma, Y.; Chen, C. Org. Chem. Front. 2014, 1, 468.
[53]
Zhang, X.; Guo, S.; Tang, P. Org. Chem. Front. 2015, 2, 806.
[54]
Aschmann, S. M.; Atkinson, R. Int. J. Chem. Kinet. 1995, 27, 613.
[55]
Russell, G. A. J. Am. Chem. Soc. 1958, 80, 4987.
[56]
Russell, G. A. J. Am. Chem. Soc. 1958, 80, 5002.
[57]
Dneprovskii, A. S.; Kuznetsov, D. V.; Eliseenkov, E. V.; Fletcher, B.; Tanko, J. M. J. Org. Chem 1998, 63, 8860.
[58]
Sutradhar, D.; Zeegers-Huyskens, T.; Chandra, A. K. Mol. Phys. 2015, 113, 3232.
[59]
Sumiyoshi, T.; Minegishi, H.; Fujiyoshi, R.; Sawamura, S. Chem. Lett. 2005, 34, 794.
[60]
Dooley, D. M.; Landin, J. A.; Rosenzweig, A. C.; Zumft, W. G.; Day, E. P. J. Am. Chem. Soc. 1991, 113, 8978.
[61]
Breslow, R.; Wiedenfeld, D. Tetrahedron Lett. 1993, 34, 1107.
[62]
Breslow, R.; Guo, T. Tetrahedron Lett. 1987, 28, 3187.
[63]
Jia, P.; Li, Q.; Poh, W. C.; Jiang, H.; Liu, H.; Deng, H.; Wu, J. Chem 2020, 6, 1766.
[64]
An, Q.; Wang, Z.; Chen, Y.; Wang, X.; Zhang, K.; Pan, H.; Liu, W.; Zuo, Z. J. Am. Chem. Soc. 2020, 142, 6216.
[65]
Cao, H.; Kong, D.; Yang, L.-C.; Chanmungkalakul, S.; Liu, T.; Piper, J. L.; Peng, Z.; Gao, L.; Liu, X.; Hong, X.; Wu, J. Nat. Synth. 2022, 1, 794.
[66]
Zheng, C.-Y.; Yue, J.-M. Nat. Commun. 2023, 14, 2399.
[67]
Bull, J. A.; Mousseau, J. J.; Pelletier, G.; Charette, A. B. Chem. Rev. 2012, 112, 2642.
[68]
Wang, B.; Pettenuzzo, C. A.; Singh, J.; Mccabe, G. E.; Clark, L.; Young, R.; Pu, J.; Deng, Y. ACS Catal. 2022, 12, 10441.
[69]
Zard, S. Z. Chem. Soc. Rev. 2008, 37, 1603.
[70]
Jeffrey, J. L.; Terrett, J. A.; MacMillan, D. W. C. Science 2015, 349, 1532.
[71]
Le, C.; Liang, Y.; Evans, R. W.; Li, X.; MacMillan, D. W. C. Nature 2017, 547, 79.
[72]
Matsumoto, A.; Yamamoto, M.; Maruoka, K. ACS Catal. 2022, 12, 2045.
[73]
Panferova, L. I.; Zubkov, M. O.; Kokorekin, V. A.; Levin, V. V.; Dilman, A. D. Angew. Chem., Int. Ed. 2021, 60, 2849.
[74]
Zachmann, A.; Drappeau, J.; Liu, S.; Alexanian, E. J. Angew. Chem., Int. Ed. 2024, 63, e202404879.
[75]
Zhang, Q.; An, B.; Lei, Y.; Gao, Z.; Zhang, H.; Xue, S.; Jin, X.; Xu, W.; Wu, Z.; Wu, M.; Yang, X.; Wu, W. Angew. Chem., Int. Ed. 2023, 62, e202304699.
[76]
Tzirakis, M. D.; Lykakis, I. N.; Orfanopoulos, M. Chem. Soc. Rev. 2009, 38, 2609.
[77]
N. Lykakis,, I.; Evgenidou, E.; Orfanopoulos, M. Curr. Org. Chem. 2012, 16, 2400.
[78]
Lazzaroni, S.; Ravelli, D.; Protti, S.; Fagnoni, M.; Albini, A. C. R. Chim. 2017, 20, 261.
[79]
Wang, Q.; Ni, S.; Yu, L.; Pan, Y.; Wang, Y. ACS Catal. 2022, 12, 11071.
[80]
Wang, Q.; Ni, S.; Wang, X.; Wang, Y.; Pan, Y. Sci. China: Chem. 2022, 65, 678.
[81]
Li, G.-X.; Hu, X.; He, G.; Chen, G. ACS Catal. 2018, 8, 11847.
[82]
Deno, N. C.; Gladfelter, E. J.; Pohl, D. G. J. Org. Chem. 1979, 44, 3728.
[83]
McMillan, A. J.; Sieńkowska, M.; Lorenzo, P. D.; Gransbury, G. K.; Chilton, N. F.; Salamone, M.; Ruffoni, A.; Bietti, M.; Leonori, D. Angew. Chem., Int. Ed. 2021, 60, 7132.
[84]
Lu, Z.-P.; Ju, M.; Wang, Y.; Meinhardt, J. M.; Martinez, J. I.; Villemure, E.; Terrett, J. A.; Lin, S. Nature 2023, 619, 514.
[85]
Schmidt, V. A.; Quinn, R. K.; Brusoe, A. T.; Alexanian, E. J. J. Am. Chem. Soc. 2014, 136, 14389.
[86]
Liu, Y.; Shi, B.; Zhao, L.; Gao, R.; Huang, C.; Alhumade, H.; Wang, S.; Qi, X.; Lei, A. J. Am. Chem. Soc. 2021, 143, 20863.
[87]
Carestia, A. M.; Ravelli, D.; Alexanian, E. J. Chem. Sci. 2018, 9, 5360.
[88]
Wang, Z.; Wang, F. Chin. J. Chem. 2022, 40, 1751.
[89]
Gonzalez, M. I.; Gygi, D.; Qin, Y.; Zhu, Q.; Johnson, E. J.; Chen, Y.-S.; Nocera, D. G. J. Am. Chem. Soc. 2022, 144, 1464.
[90]
Shu, C.; Noble, A.; Aggarwal, V. K. Nature 2020, 586, 714.
[91]
Sang, R.; Han, W.; Zhang, H.; Saunders, C. M.; Noble, A.; Aggarwal, V. K. J. Am. Chem. Soc. 2023, 145, 15207.
[92]
Tu, J.-L.; Hu, A.-M.; Guo, L.; Xia, W. J. Am. Chem. Soc. 2023, 145, 7600.
[93]
Zhong, P.-F.; Tu, J.-L.; Zhao, Y.; Zhong, N.; Yang, C.; Guo, L.; Xia, W. Nat. Commun. 2023, 14, 6530.
[94]
Cao, Y.; Huang, C.; Lu, Q. Nat. Synth. 2024, 3, 537.
[95]
Wei, W.; Wang, B.; Hom?lle, S. L.; Zhu, J.; Li, Y.; Münchow, T. von; Maksso, I.; Ackermann, L. CCS Chem. 2024, 6, 1430.
[96]
Fang, W.; Wang, H.-Q.; Zhou, W.; Luo, Z.-W.; Dai, J.-J. Chem. Commun. 2023, 59, 7108.
[97]
Wang, M.; Huang, Y.; Hu, P. Science 2024, 383, 537.
[98]
Jin, Y.; Wang, L.; Zhang, Q.; Zhang, Y.; Liao, Q.; Duan, C. Green Chem. 2021, 23, 9406.
[99]
Zou, L.; Xiang, S.; Sun, R.; Lu, Q. Nat. Commun. 2023, 14, 7992.
[100]
Li, Q.-Y.; Cheng, S.; Ye, Z.; Huang, T.; Yang, F.; Lin, Y.-M.; Gong, L. Nat. Commun. 2023, 14, 6366.
[101]
Takahira, Y.; Chen, M.; Kawamata, Y.; Mykhailiuk, P.; Nakamura, H.; Peters, B. K.; Reisberg, S. H.; Li, C.; Chen, L.; Hoshikawa, T.; Shibuguchi, T.; Baran, P. S. Synlett 2019, 30, 1178.
[102]
Saito, M.; Kawamata, Y.; Meanwell, M.; Navratil, R.; Chiodi, D.; Carlson, E.; Hu, P.; Chen, L.; Udyavara, S.; Kingston, C.; Tanwar, M.; Tyagi, S.; McKillican, B. P.; Gichinga, M. G.; Schmidt, M. A.; Eastgate, M. D.; Lamberto, M.; He, C.; Tang, T.; Malapit, C. A. J. Am. Chem. Soc. 2021, 143, 7859.
[103]
Zou, L.; Wang, X.; Xiang, S.; Zheng, W.; Lu, Q. Angew. Chem., Int. Ed. 2023, 62, e202301026.
[104]
Dai, Z.-Y.; Nong, Z.-S.; Song, S.; Wang, P.-S. Org. Lett. 2021, 23, 3157.
[105]
Jin, Y.; Fan, L.-F.; Wang, E.; Yu, L.; Hirao, H.; Gong, L.-Z. J. Am. Chem. Soc. 2023, 145, 22031.
[106]
Ge, L.; Wang, H.; Liu, Y.; Feng, X. J. Am. Chem. Soc. 2024, 146, 13347.
[107]
Ruan, X.-Y.; Wu, D.-X.; Li, W.-A.; Lin, Z.; Sayed, M.; Han, Z.-Y.; Gong, L.-Z. J. Am. Chem. Soc. 2024, 146, 12053.
文章导航

/