Chinese Journal of Organic Chemistry ›› 2024, Vol. 44 ›› Issue (11): 3321-3334.DOI: 10.6023/cjoc202403011 Previous Articles Next Articles
REVIEW
郑威, 刘凤雪, 赵红琼, 许颖, 陈宁*(), 刘颖杰*()
收稿日期:
2024-04-30
修回日期:
2024-05-23
发布日期:
2024-06-13
基金资助:
Wei Zheng, Fengxue Liu, Hongqiong Zhao, Ying Xu, Ning Chen*(), Yingjie Liu*()
Received:
2024-04-30
Revised:
2024-05-23
Published:
2024-06-13
Contact:
*E-mail:Supported by:
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Wei Zheng, Fengxue Liu, Hongqiong Zhao, Ying Xu, Ning Chen, Yingjie Liu. Recent Progress on Methods for the Preparation of Mono/Di/Trifluoromethoxylation Reagents[J]. Chinese Journal of Organic Chemistry, 2024, 44(11): 3321-3334.
[1] |
Ni C.; Hu J. Chem. Soc. Rev. 2016, 45, 5441.
|
[2] |
Liang T.; Neumann C. N.; Ritter T. Angew. Chem., nt. Ed. 2013, 52, 8214.
|
[3] |
Cheng M.; Guo C.; Gross M. L. Angew. Chem., nt. Ed. 2020, 59, 5880.
|
[4] |
Hu J. B. Acta Chim. Sinica 2024, 82, 103 (in Chinese).
|
(胡金波, 化学学报, 2024, 82, 103.)
doi: 10.6023/A2024E001 |
|
[5] |
(a) Leroux F.; Jeschke P.; Schlosser M. Chem. Rev. 2005, 105, 827.
|
(b) Jeschke P.; Baston E.; Leroux F. R. Mini Rev. Med. Chem. 2007, 7, 10274.
|
|
(c) Manteau B.; Pazenok S.; Vors J. P.; Leroux F. R. J. Fluorine Chem. 2010, 131, 140.
|
|
[6] |
Donohue S. R.; Krushinski J. H.; Pike V. W.; Chernet E.; Phebus L.; Chesterfield A. K.; Felder C. C.; Halldin C.; Schaus J. M. J. Med. Chem. 2008, 51, 5833.
doi: 10.1021/jm800416m pmid: 18800770 |
[7] |
Xing L.; Blakemore D. C.; Narayanan A.; Unwalla R.; Lovering F.; Denny R. A.; Zhou H.; Bunnage M. E. Chem. Med. Chem. 2015, 10, 715.
|
[8] |
Dolbier W. R. Jr; Battiste M. A. Chem. Rev. 2003, 103, 1071.
|
[9] |
Zhu J.; Liu Y.; Shen Q. Angew. Chem., nt. Ed. 2016, 55, 9050.
|
[10] |
Si Y.; Tang P. Chin. J. Chem. 2023, 41, 2179.
|
[11] |
Leo A.; Hansch C.; Elkins D. Chem. Rev. 1971, 71, 525.
|
[12] |
Hansch C.; Leo A.; Taft R. W. Chem. Rev. 2002, 91, 165.
|
[13] |
Federsel D.; Herrmann A.; Christen D.; Sander S.; Willner H.; Oberhammer H. Mol. Struct. 2001, 567, 127.
|
[14] |
Li X; Blakemore D. C.; Arjun N.; Ray U.; Frank L.; Aldrin R. D.; Zhou H. Y.; Bunnage M. E. ChemMedChem 2015, 10, 715.
|
[15] |
Iwata R.; Furumoto S.; Pascali C.; Anna P. B.; Ishiwata K. J. Labelled Compd. Radiopharm. 2003, 46, 555.
|
[16] |
Iwata R.; Pascali C.; Bogni A.; Furumoto S.; Terasaki K.; Yanai K. Appl. Radiat. Isot. 2002, 57, 347.
|
[17] |
Ramkumar N.; Sperga A.; Belyakov S.; Mishnev A.; Zacs D.; Veliks J. Adv. Synth. Catal. 2023, 365, 1405.
|
[18] |
Sperga A.; Melngaile R.; Kazia A.; Belyakov S.; Veliks J. J. Org. Chem. 2021, 86, 3196.
|
[19] |
(a) Sperga A.; Kazia A.; Veliks J. Org. Biomol. Chem. 2021, 19, 2688.
|
(b) Sperga A.; Zacs D.; Veliks J. Org. Lett. 2022, 24, 4474.
|
|
[20] |
Bertoli G.; Martínez Á. M.; Goebel J. F.; Belmonte D.; Sivendran N.; Gooßen L. Angew. Chem. 2022, 135, 1405.
|
[21] |
Ni C.; Hu J. Synthesis 2014, 46, 842.
|
[22] |
Li J.; Smith D.; Krishnananthan S. Org. Process Res. Dev. 2012, 16, 156.
|
[23] |
Tao Z.-F.; Sowin T. J.; Lin N.-H. Synlett 2007, 18, 2855.
|
[24] |
Lee W. J.; Zheng W.; Morales-Rivera A. C.; Liu P.; Ngai M. Y. Chem. Sci. 2019, 10, 3217.
|
[25] |
Lee J. W.; Lim S.; Maienshein D. N.; Liu P.; Ngai M. Y. Angew. Chem. 2020, 132, 21659.
|
[26] |
Zheng W. J.; Lee J. W.; Morales-Rivera C. A.; Liu P.; Ngai M. Y. Angew. Chem., nt. Ed. 2018, 57, 13795.
|
[27] |
Lin D.; Prakash G. K. S. Org. Lett. 2022, 24, 7707.
|
[28] |
Lee K. N.; Lee J. W.; Ngai M. Y. Tetrahedron 2018, 74, 7127.
|
[29] |
Huang C. H.; Liang T.; Harada S.; Lee E.; Ritter T. J. Am. Chem. Soc. 2011, 133, 13308.
|
[30] |
Guo S.; Cong F.; Guo R.; Wang L.; Tang P. P. Nat. Chem. 2017, 9, 546.
|
[31] |
Türksoy A.; Leonori D.; Klankermayer J.; Schoenebeck F. Ph.D. Dissertation, Universitätsbibliothek der RWTH Aachen, Yozgat 2023.
|
[32] |
Jiang X.; Tang P. Chin. J. Chem. 2021, 39, 255.
|
[33] |
Zhou M.; Ni C. F.; He Z. B.; Hu J. B. Org. Lett. 2016, 18, 3754.
doi: 10.1021/acs.orglett.6b01779 pmid: 27440264 |
[34] |
Umemoto T.; Adachi K.; Ishihara S. J. Org. Chem. 2007, 72, 6905.
pmid: 17676906 |
[35] |
Jelier B. J.; Howell J. L.; Montgomery C. D.; Leznoff D. B.; Friesen C. M. Angew. Chem., nt. Ed. 2015, 54, 2945.
|
[36] |
Tlili A.; Toulgoat F.; Billard T. Angew. Chem., nt. Ed. 2016, 55, 11726.
|
[37] |
Besset T.; Jubault P.; Pannecoucke X.; Poisson T. Org. Chem. Front. 2016, 3, 1004.
|
[38] |
Hao B. Y.; Han Y. P.; Zhang Y.; Liang Y. M. Org. Biomol. Chem. 2023, 21, 4926.
|
[39] |
Pelaez W. J.; Arguello G. A. Tetrahedron Lett. 2010, 51, 5242.
|
[40] |
Kellogg K. B.; Cady G. H. J. Am. Chem. Soc. 1948, 70, 3986.
|
[41] |
Porter R. S.; Cady G. H. J. Am. Chem. Soc. 1957, 79, 5625.
|
[42] |
Barton D. H.; Hesse R. H.; Jackman G. P.; Pechet M. M. J. Chem. Soc., Perkin Trans. 1 1977, 2604.
|
[43] |
Francesco V.; Sansotera M.; Navarrini W. J. Fluorine Chem. 2013, 155, 2.
|
[44] |
Schack C. J.; Maya W. J. Am. Chem. Soc. 1969, 91, 2902.
|
[45] |
Porter R. S.; Cady G. H. J. Am. Chem. Soc. 1957, 79, 5628.
|
[46] |
Ginsburg V. A.; Vlasova E. S.; Vasil'eva M. N.; Mirzabekova N. Y. S.; Makarov S. P.; Shchekotikhin A. I.; Yakubovich A. Y. Dokl. Akad. Nauk 1963, 149, 97.
|
[47] |
Thompson P. G. J. Am. Chem. Soc. 1967, 89, 4316.
|
[48] |
Anderson L. R.; Fox W. B. J. Am. Chem. Soc. 1967, 89, 4313.
|
[49] |
Matoušek V.; Pietrasiak E.; Sigrist L.; Czarniecki B.; Togni A. Eur. J. Org. Chem. 2014, 2014, 3087.
|
[50] |
Liang A.; Han S.; Liu Z.; Wang L.; Li J.; Zou D.; Wu Y.; Wu Y. Chem. Eur. J. 2016, 22, 5102.
|
[51] |
Yuan W. J.; Tong C. L.; Xu X. H.; Qing F. L. J. Org. Chem. 2023, 88, 4434.
|
[52] |
Jelier B. J.; Tripet P. F.; Pietrasiak E.; Franzoni I.; Jeschke G.; Togni A. Angew. Chem., nt. Ed. 2018, 57, 13784.
|
[53] |
Zheng W.; Morales-Rivera C. A.; Lee J. W.; Liu P.; Ngai M. Y. Angew. Chem. 2018, 130, 9793.
|
[54] |
Zheng W.; Lee J. W.; Morales-Rivera C. A.; Liu P.; Ngai M. Y. Angew. Chem., Int. Ed. 2018, 57, 13795.
|
[55] |
Huang C.; Liang T.; Harada S.; Lee E.; Ritter T. J. Am. Chem. Soc. 2011, 133, 13308.
|
[56] |
Chen S.; Huang Y.; Fang X.; Li H.; Zhang Z.; Hor T. A.; Weng Z. Dalton Trans. 2015, 44, 19682.
|
[57] |
Guo S.; Cong F.; Guo R.; Wang L.; Tang P. Nat. Chem. 2017, 9, 546.
|
[58] |
Koller R.; Huchet Q.; Battaglia P.; Welch J. M.; Togni A. Chem. Commun. 2009, 5993.
|
[59] |
Li Y.; Yang Y.; Xin J.; Tang P. Nat. Commun. 2020, 11, 755.
doi: 10.1038/s41467-020-14598-1 pmid: 32029731 |
[60] |
Huang W. C.; Wan X. L.; Shen Q. L. Angew. Chem. 2017, 129, 12148.
|
[61] |
Marrec O.; Billard T.; Vors J.-P.; Pazenok S.; Longlois B. R. J. Fluorine Chem. 2010, 131, 200.
|
[62] |
Chen D.; Lu L.; Shen Q. Org. Chem. Front. 2019, 6, 1801.
|
[63] |
Olah G.A.; Ohyama T. Synthesis 1976 5, 319.
|
[64] |
Noftle R. E. Inorg. Nucl. Chem. Lett. 1980, 16, 195.
|
[65] |
Noftle R. E.; Cady G. H. Inorg. Chem. 1965, 4, 1010.
|
[66] |
Katsuhara Y.; DesMarteau D. D. J. Am. Chem. Soc. 1980, 102, 2681.
|
[67] |
Kobayashi Y.; Yoshida T.; Kumadaki I. Tetrahedron Lett. 1979, 20, 3865.
|
[68] |
Engelbrecht V. A.; Tschager E. Z. Anorg. Allg. Chem. 1977, 433, 19.
|
[69] |
Hassani M.O.; Germain A.; Brunel D.; Commeyras A. Tetrahedron Lett. 1981, 22, 65.
|
[70] |
Taylor S. L.; Martin J. C. J. Org. Chem. 1987, 52, 4147.
|
[71] |
Zhang Q. W.; Hartwig J. F. Chem. Commun. 2018, 54, 10124.
|
[72] |
Zhou M.; Ni C. F.; Zeng Y. W.; Hu J. B. J. Am. Chem. Soc. 2018, 140, 6801.
doi: 10.1021/jacs.8b04000 pmid: 29787259 |
[73] |
Turksoy A.; Scattolin T.; Bouayad-Gervais S.; Schoenebeck F. Chem.-Eur. J. 2020, 26, 2183.
|
[74] |
(a) Chen C.; Chen P.; Liu G. J. Am. Chem. Soc. 2015, 137, 15648.
pmid: 30240641 |
(b) Chen C.; Luo Y.; Fu L.; Chen P.; Lan Y.; Liu G. J. Am. Chem. Soc. 2018, 140, 1207.
pmid: 30240641 |
|
(c) Zhang C.-P.; Vicic D. A. Organometallics 2012, 31, 7812.
pmid: 30240641 |
|
(d) Chen S.; Huang Y.; Fang X.; Li H.; Zhang Z.; Hor T. S.; Weng Z. Dalton Trans. 2015, 44, 19682.
pmid: 30240641 |
|
(e) Zhang W.; Chen J.; Lin J. H.; Xiao J. C.; Gu Y. C. iScience 2018, 5, 110.
doi: S2589-0042(18)30092-0 pmid: 30240641 |
|
(f) Zha G. F.; Han J. B.; Hu X. Q.; Qin H. L.; Fang W. Y.; Zhang C. P. Chem. Commun. 2016, 52, 7458.
pmid: 30240641 |
|
(g) Wang Q.; Zhang X.; Sorochinsky A. E.; Butler G.; Han J.; Soloshonok V. A. Symmetry 2021, 13, 2380.
pmid: 30240641 |
|
(h) Cong F.; Wei Y.; Tang P. Chem. Commun. 2018, 54, 4473.
pmid: 30240641 |
|
(i) Yang H.; Wang F.; Jiang X.; Zhou Y.; Xu X.; Tang P. Angew. Chem., nt. Ed. 2018, 57, 13266.
pmid: 30240641 |
|
(j) Wang F.; Xu P.; Cong F.; Tang P. Chem. Sci. 2018, 9, 8836.
pmid: 30240641 |
|
[75] |
Kolomeitsev A. A.; Vorobyev M.; Gillandt H. Tetrahedron Lett. 2008, 49, 449.
|
[76] |
Petzold D.; Nitschke P.; Brandl F.; Scheidler V.; Dick B.; Gschwind R. M.; König B. Chem.-Eur J. 2019, 25, 361.
doi: 10.1002/chem.201804603 pmid: 30216578 |
[77] |
Duran-Camacho G.; Ferguson D. M.; Kampf J. W.; Bland D. C.; Sanford M. S. Org. Lett. 2021, 23, 5138.
|
[78] |
Lu Z.; Kumon T.; Hammond G. B.; Umemoto T. Angew. Chem., nt. Ed. 2021, 60, 16171.
|
[79] |
Umemoto T.; Zhang B.; Zhu T.; Zhou X.; Zhang P.; Hu S.; Li Y. J. Org. Chem. 2017, 82, 7708.
doi: 10.1021/acs.joc.7b00669 pmid: 28541682 |
[80] |
Kondo H.; Maeno M.; Hirano K.; Shibata N. Chem. Commun. 2018, 54, 5522.
|
[81] |
(a) Behenna D. C.; Liu Y.; Yurino T.; Kim J.; White D. E.; Virgil S. C.; Stoltz B. M. Nat. Chem. 2012, 4, 130.
|
(b) Korch K. M.; Eidamshaus C.; Behenna D. C.; Nam S.; Horne D.; Stoltz B. M. Angew. Chem., nt. Ed. 2015, 54, 179.
|
|
(c) Numajiri Y.; JiménezOsés G.; Wang B.; Houk K. N.; Stoltz B. M. Org. Lett. 2015, 17, 1082.
|
|
(d) Kita Y.; Numajiri Y.; Okamoto N.; Stoltz B. M. Tetrahedron 2015, 71, 6349.
|
|
[82] |
Liu J. B.; Xu X. H.; Qing F. L. Org. Lett. 2015, 17, 5048.
|
[83] |
Newton J. J.; Jelier B. J.; Meanwell M.; Martin R. E.; Britton R.; Friesen C. M. Org. Lett. 2020, 22, 1785.
|
[84] |
Kolomeitsev A. A.; Vorobyev M.; Gillandt H. Tetrahedron Lett. 2007, 49, 449.
|
[85] |
Chen D.; Luo Y.; Lu L.; Shen Q. Organometallics 2024, DOI: 10.1021/acs.organomet.4c00073.
|
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